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- 2024
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Mark
Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young—FGF-21 Highly Associated with Overt Disease
(
- Contribution to journal › Article
-
Mark
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
(
- Contribution to journal › Article
-
Mark
Frailty and Cognitive Function in Middle-Aged and Older Adults With Congenital Heart Disease
(
- Contribution to journal › Article
-
Mark
Genetic correlations and causal relationships between cardio-metabolic traits and sepsis
(
- Contribution to journal › Article
-
Mark
Reply to “Exploring the long-term effects of biologic initiation in severe asthma: Insights from the International Severe Asthma Registry”
(
- Contribution to journal › Article
-
Mark
A genome-wide association study of social trust in 33,882 Danish blood donors
(
- Contribution to journal › Article
- 2023
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Mark
Is asthma's heterogeneity too vast to use traditional phenotyping for modern biologic therapies?
(
- Contribution to journal › Article
-
Mark
Early onset ataxia with comorbid myoclonus and epilepsy : A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement
(
- Contribution to journal › Article
-
Mark
Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome
(
- Contribution to journal › Article
-
Mark
Clusters based on immune markers in a Lithuanian asthma cohort study
(
- Contribution to journal › Article
-
Mark
Phenotype of Gambling Disorder Patients with Lotteries as a Preferred Form of Gambling
(
- Contribution to journal › Article
-
Mark
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
(
- Contribution to journal › Article
-
Mark
Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalization
(
- Contribution to journal › Article
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Mark
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
(
- Contribution to journal › Article
-
Mark
SID : A new carbohydrate blood group system based on a well-characterized but still mysterious antigen of great pathophysiologic interest
(
- Contribution to journal › Article
- 2022
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Mark
Multiple sclerosis diagnosis and phenotype identification by multivariate classification of in vivo frontal cortex metabolite profiles
(
- Contribution to journal › Article
-
Mark
The role of phenotypic plasticity in the establishment of range margins
2022) In Philosophical transactions of the Royal Society of London. Series B, Biological sciences 377(1846).(
- Contribution to journal › Article
-
Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
-
Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
(
- Contribution to journal › Article
-
Mark
A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B
w phenotype.
(
- Contribution to journal › Article
-
Mark
International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery
(
- Contribution to journal › Article
-
Mark
phenopype : A phenotyping pipeline for Python
(
- Contribution to journal › Article
-
Mark
Computational phenotyping of obstructive airway diseases : protocol for a systematic review
(
- Contribution to journal › Article
-
Mark
Life histories as mosaics : Plastic and genetic components differ among traits that underpin life-history strategies
(
- Contribution to journal › Article
- 2021
-
Mark
Treatment outcomes in persons with severe haemophilia B in the Nordic region : The B-NORD study
(
- Contribution to journal › Article
-
Mark
Synovial fluid neutrophils in oligoarticular juvenile idiopathic arthritis have an altered phenotype and impaired effector functions
(
- Contribution to journal › Article
-
Mark
The European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)-clinical phenotypes and their predictors based on a cohort of 1000 patients
(
- Contribution to journal › Article
-
Mark
Congenital stationary night blindness : an update and review of the disease spectrum in Saudi Arabia
(
- Contribution to journal › Scientific review
-
Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
(
- Contribution to journal › Article
-
Mark
AXL Knock-Out in SNU475 Hepatocellular Carcinoma Cells Provides Evidence for Lethal Effect Associated with G2 Arrest and Polyploidization
(
- Contribution to journal › Article
- 2020
-
Mark
Myoclonus-dystonia (DYT11, DYT-SGCE) - a channelopathy?
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Diffusion-Weighted Imaging, MR Angiography, and Baseline Data in a Systematic Multicenter Analysis of 3,301 MRI Scans of Ischemic Stroke Patients—Neuroradiological Review Within the MRI-GENIE Study
(
- Contribution to journal › Article
-
Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
(
- Contribution to journal › Article
-
Mark
A Functional Genomic Screen Identifies the Deubiquitinase USP11 as a Novel Transcriptional Regulator of ERα in Breast Cancer
(
- Contribution to journal › Article
-
Mark
Three-dimensional single-cell imaging for the analysis of RNA and protein expression in intact tumour biopsies
(
- Contribution to journal › Article
-
Mark
SSD1 modifies phenotypes of Elongator mutants
(
- Contribution to journal › Scientific review
- 2019
-
Mark
Gene transfer by interspecific hybridization in bryophytes
2019)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)
(
- Contribution to journal › Article
-
Mark
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Phenotype prediction accuracy – A Swedish perspective
(
- Contribution to journal › Article
-
Mark
SSD1 suppresses phenotypes induced by the lack of Elongator-dependent tRNA modifications
(
- Contribution to journal › Article
- 2018
-
Mark
Molecular subtype profiling of urothelial carcinoma using a subtype-specific immunohistochemistry panel
(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Contrasting results from GWAS and QTL mapping on wing length in great reed warblers
(
- Contribution to journal › Article
-
Mark
Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum Disorder
(
- Contribution to journal › Article
-
Mark
Towards precision medicine in severe asthma : Treatment algorithms based on treatable traits
(
- Contribution to journal › Scientific review
-
Mark
Timing of onset affects arthritis presentation pattern in antisynthetase syndrome
(
- Contribution to journal › Article
-
Mark
A response to the forensic genetics policy initiative's report "Establishing Best Practice for Forensic DNA Databases"
(
- Contribution to journal › Letter
- 2017
-
Mark
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
(
- Contribution to journal › Article
-
Mark
The P1 histo-blood group antigen is present on human red blood cell glycoproteins
2017) 27th Regional Congress of the International Society of Blood Transfusion, ISBT 2017 In Vox Sanguinis 112(S1). p.25-25(
- Contribution to journal › Published meeting abstract
-
Mark
Pyk2 inhibition promotes contractile differentiation in arterial smooth muscle
(
- Contribution to journal › Article
-
Mark
Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12
(
- Contribution to journal › Article
-
Mark
PBB3 Imaging in Parkinsonian disorders: Evidence for binding to abnormally aggregated proteins in addition to tau proteins
2017) 21st International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 32(Suppl 2). p.585-587(
- Contribution to journal › Published meeting abstract
-
Mark
Regulation of microRNA expression in vascular smooth muscle by MRTF-A and actin polymerization
(
- Contribution to journal › Article
-
Mark
Do group dynamics affect colour morph clines during a range shift?
(
- Contribution to journal › Article
-
Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- Contribution to journal › Article
-
Mark
Systemic frequencies of T helper 1 and T helper 17 cells in patients with age-related macular degeneration : A case-control study
(
- Contribution to journal › Article
-
Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
-
Mark
Acute doses of caffeine shift nervous system cell expression profiles toward promotion of neuronal projection growth
(
- Contribution to journal › Article
-
Mark
Knee internal contact force in a varus malaligned phenotype in knee osteoarthritis (KOA)
(
- Contribution to journal › Article
- 2016
-
Mark
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
(
- Contribution to journal › Article
-
Mark
CCoAOMT Down-Regulation Activates Anthocyanin Biosynthesis in Petunia
(
- Contribution to journal › Article
-
Mark
Heterozygous PINK1 p.G411S mutation increases risk for Parkinson's disease (PD)
2016) 20th International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 31(Suppl. S2). p.282-282(
- Contribution to journal › Published meeting abstract
-
Mark
Synovitis and radiographic progression in non-erosive and erosive hand osteoarthritis : is erosive hand osteoarthritis a separate inflammatory phenotype?
(
- Contribution to journal › Article
-
Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
-
Mark
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
(
- Contribution to journal › Article
-
Mark
Tuning fresh : radiation through rewiring of central metabolism in streamlined bacteria
(
- Contribution to journal › Article
-
Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- Contribution to journal › Article
-
Mark
Identification of clinical phenotypes in knee osteoarthritis : a systematic review of the literature
(
- Contribution to journal › Article
- 2015
-
Mark
Obesity and asthma: current knowledge and future needs
(
- Contribution to journal › Scientific review
-
Mark
Tracking Parkinson's : Study Design and Baseline Patient Data
(
- Contribution to journal › Article
-
Mark
miR-155, identified as anti-metastatic by global miRNA profiling of a metastasis model, inhibits cancer cell extravasation and colonization in vivo and causes significant signaling alterations
(
- Contribution to journal › Article
-
Mark
Fell-Muir Lecture : Syndecans: from peripheral coreceptors to mainstream regulators of cell behaviour
(
- Contribution to journal › Scientific review
-
Mark
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease
(
- Contribution to journal › Article
- 2014
-
Mark
Prospective observational cohort studies for studying rare diseases: the European PedNet Haemophilia Registry
(
- Contribution to journal › Article
-
Mark
A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
(
- Contribution to journal › Article
-
Mark
Human anaplastic thyroid carcinoma cells are sensitive to NK cell-mediated lysis via ULBP2/5/6 and chemoattract NK cells
(
- Contribution to journal › Article
-
Mark
Transgenic expression of constitutively active RAC1 disrupts mouse rod morphogenesis
(
- Contribution to journal › Article
-
Mark
IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes
(
- Contribution to journal › Article
-
Mark
The mitochondrial outer membrane AAA ATPase AtOM66 affects cell death and pathogen resistance in Arabidopsis thaliana
(
- Contribution to journal › Article
-
Mark
Triggering necroptosis in cisplatin and IAP antagonist-resistant ovarian carcinoma
(
- Contribution to journal › Article
-
Mark
1,25-Dihydroxyvitamin D3 promotes tolerogenic dendritic cells with functional migratory properties in NOD mice
(
- Contribution to journal › Article
-
Mark
The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
(
- Contribution to journal › Article
- 2013
-
Mark
Phenotypic map of porcine retinal ganglion cells
(
- Contribution to journal › Article
-
Mark
GNAL mutations cause adult-onset primary dystonia
(
- Contribution to journal › Published meeting abstract
-
Mark
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders
(
- Contribution to journal › Article
-
Mark
A membrane-bound NAC transcription factor, ANAC017, mediates mitochondrial retrograde signaling in Arabidopsis
(
- Contribution to journal › Article
- 2012
-
Mark
Characterization of mutations in barley fch2 encoding chlorophyllide a oxygenase
(
- Contribution to journal › Article
-
Mark
Induced mutations in circadian clock regulator Mat-a facilitated short-season adaptation and range extension in cultivated barley
(
- Contribution to journal › Article
-
Mark
Hybrid zone dynamics, assortative mating, and migratory programmes in a willow warbler migratory divide
2012)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Lactobacillus reuteri prevents diet-induced obesity, but not atherosclerosis, in a strain dependent fashion in Apoe-/- mice
(
- Contribution to journal › Article
-
Mark
Advantages and limitations of different p62-based assays for estimating autophagic activity in Drosophila
(
- Contribution to journal › Article
- 2011
-
Mark
Asthma endotypes: A new approach to classification of disease entities within the asthma syndrome
(
- Contribution to journal › Article
-
Mark
Signs of Degeneration in 12-22-Year Old Grafts of Mesencephalic Dopamine Neurons in Patients with Parkinson's Disease
(
- Contribution to journal › Article
-
Mark
Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium
(
- Contribution to journal › Article
-
Mark
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
(
- Contribution to journal › Article
-
Mark
Draft genome of the red harvester ant Pogonomyrmex barbatus
2011) In Proceedings of the National Academy of Sciences of the United States of America 108(14). p.5667-5672(
- Contribution to journal › Article
- 2010
-
Mark
MicroRNAs are necessary for vascular smooth muscle growth, differentiation, and function
(
- Contribution to journal › Article
-
Mark
Glycomic and transcriptomic response of GSC11 glioblastoma stem cells to STAT3 phosphorylation inhibition and serum-induced differentiation
(
- Contribution to journal › Article
-
Mark
Familial late-onset focal dystonia in an African American family
(
- Contribution to journal › Published meeting abstract
-
Mark
Specific genomic aberrations in primary colorectal cancer are associated with liver metastases
(
- Contribution to journal › Article
- 2009
-
Mark
The plasma concentration of activated protein C appears normal in patients with haemophilia
(
- Contribution to journal › Article
-
Mark
MC1R variation and melanoma risk in the Swedish population in relation to clinical and pathological parameters
(
- Contribution to journal › Article
- 2008
-
Mark
Abnormal cytoskeletal protein expression in cultured skin fibroblasts form type 1 diabetes mellitus patiens with nephropathy: A proteomic approach
(
- Contribution to journal › Article
-
Mark
Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis
(
- Contribution to journal › Article
-
Mark
Functional importance of individual rRNA 2'-O-ribose methylations revealed by high-resolution phenotyping
(
- Contribution to journal › Article
-
Mark
U-2973, a novel B-cell line established from a patient with a mature B-cell leukemia displaying concurrent t(14;18) and MYC translocation to a non-IG gene partner.
(
- Contribution to journal › Article
-
Mark
Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles
(
- Contribution to journal › Article
-
Mark
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration
(
- Contribution to journal › Article
-
Mark
Enterohemorrhagic Escherichia coli O157:H7 isolates from children in Cuba
(
- Contribution to journal › Letter
- 2007
-
Mark
Studies on the genetic basis of Pk, P and P1 blood group antigen expression
2007)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Analysis of ocular hypopigmentation in Rab38cht/cht mice
(
- Contribution to journal › Article
-
Mark
Mitochondrial type-I prohibitins of Arabidopsis thaliana are required for supporting proficient meristem development
(
- Contribution to journal › Article
-
Mark
CDG-Id in two siblings with partially different phenotypes
(
- Contribution to journal › Article
-
Mark
Association of yeast Upf1p with direct substrates of the NMD pathway
2007) In Proceedings of the National Academy of Sciences of the United States of America 104(52). p.7-20872(
- Contribution to journal › Article
- 2006
-
Mark
Effect of hypoxia on the tumor phenotype: the neuroblastoma and breast cancer models
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Prevalence and genetic and environmental influences on anxiety disorders in 6-year-old twins
(
- Contribution to journal › Article
-
Mark
Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts
(
- Contribution to journal › Article
- 2005
-
Mark
Blood group genotype analysis for the quality improvement of reagent test red blood cells
(
- Contribution to journal › Article
-
Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
(
- Contribution to journal › Article
-
Mark
Size of the protein-coding genome and rate of molecular evolution
(
- Contribution to journal › Article
- 2004
-
Mark
Resistens mot acetylsalicylsyra - klinisk diagnos utan klarlagd mekanism
(
- Contribution to journal › Article
-
Mark
BRCA1 och BRCA2 har nått kliniken. Tioårigt fynd av genmutation ger nu möjlighet förebygga ärftlig bröstcan
(
- Contribution to journal › Article
-
Mark
A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling.
(
- Contribution to journal › Article
- 2003
-
Mark
Morphology phenotype and ultrastructure of fibroblastic cells from normal and neuropathic human detrusor: Absence of myofibroblast characteristics
(
- Contribution to journal › Article
-
Mark
A twin study of anxiety-related behaviours in pre-school children
(
- Contribution to journal › Article
-
Mark
Discrete gene loci regulate neurodegeneration, lymphocyte infiltration, and major histocompatibility complex class II expression in the CNS
2003) In The Journal of Neuroscience : the official journal of the Society for Neuroscience 23(30). p.23-9817(
- Contribution to journal › Article
- 2002
-
Mark
Neuropathological and behavioral consequences of adeno-associated viral vector-mediated continuous intrastriatal neurotrophin delivery in a focal ischemia model in rats.
(
- Contribution to journal › Article
-
Mark
The genetic control of sialadenitis versus arthritis in a NOD.QxB10.Q F2 cross.
(
- Contribution to journal › Article
-
Mark
Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.
(
- Contribution to journal › Article
-
Mark
Hypoxia alters gene expression in human neuroblastoma cells toward an immature and neural crest-like phenotype.
(
- Contribution to journal › Article
-
Mark
Long-term survival and glial differentiation of the brain-derived precursor cell line RN33B after subretinal transplantation to adult normal rats
(
- Contribution to journal › Article
-
Mark
Thrifty genotypes and phenotypes in the pathogenesis of early-onset obesity.
(
- Contribution to journal › Letter
-
Mark
Migration patterns and phenotypic differentiation of long-term expanded human neural progenitor cells after transplantation into the adult rat brain.
(
- Contribution to journal › Article
-
Mark
Heredity of hypospadias and the significance of low birth weight
(
- Contribution to journal › Article
-
Mark
Genetic links between the acute-phase response and arthritis development in rats.
(
- Contribution to journal › Article
-
Mark
Factor V and thrombotic disease: description of a janus-faced protein.
(
- Contribution to journal › Scientific review
-
Mark
Dual function of the tRNA(m(5)U54)methyltransferase in tRNA maturation
(
- Contribution to journal › Article
- 2001
-
Mark
Clinical expressions of juvenile hereditary retinal degenerations and macular dystrophies: Electrophysiological and genetic studies
2001)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
(
- Contribution to journal › Article
- 2000
-
Mark
Sunscreen use and malignant melanoma
(
- Contribution to journal › Article
-
Mark
p53-mediated differentiation of the erythroleukemia cell line K562
(
- Contribution to journal › Article
- 1999
-
Mark
An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)
(
- Contribution to journal › Article
-
Mark
Thrombophilia as a multigenic disease
(
- Contribution to journal › Article
- 1998
-
Mark
Extracellular ATP: a growth factor for vascular smooth muscle cells
(
- Contribution to journal › Scientific review
-
Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
(
- Contribution to journal › Article
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
-
Mark
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect
(
- Contribution to journal › Article
-
Mark
Creatine kinase knockout mice - what is the phenotype : Skeletal muscle
(
- Contribution to journal › Article
-
Mark
MEN1 gene mutations in 12 MEN1 families and their associated tumors
(
- Contribution to journal › Article
- 1997
-
Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
1997)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
(
- Contribution to journal › Article
- 1996
-
Mark
PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis.
(
- Contribution to journal › Article
-
Mark
Familial thrombophilia : clinical and molecular analysis of Swedish families with inherited resistance to activated protein C or protein S deficiency
1996) In Scandinavian journal of clinical and laboratory investigation. Supplementum 56(226). p.19-46(
- Contribution to journal › Scientific review
-
Mark
Activated protein C resistance as a basis for venous thrombosis.
(
- Contribution to journal › Article
-
Mark
Differences in serum cytokine levels in acute and chronic autoimmune thrombocytopenic purpura : relationship to platelet phenotype and antiplatelet T-cell reactivity
(
- Contribution to journal › Article
- 1995
-
Mark
Phenotype variation within a choroideremia family lacking the entire CHM gene
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
(
- Contribution to journal › Article
-
Mark
Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease
(
- Contribution to journal › Article
- 1993
-
Mark
Haemophilia : strategies for carrier detection and prenatal diagnosis
(
- Contribution to journal › Article
-
Mark
Glutathione transferase activity in human vessels and in cultured arterial smooth muscle cells
(
- Contribution to journal › Article
-
Mark
An exon 5 deletion variant of the estrogen receptor frequently coexpressed with wild-type estrogen receptor in human breast cancer
(
- Contribution to journal › Article
- 1986
-
Mark
Carrier detection in hemophilia A : a cooperative international study. II. The efficacy of a universal discriminant
(
- Contribution to journal › Article
-
Mark
Carrier detection in hemophilia A : a cooperative international study. I. The carrier phenotype
(
- Contribution to journal › Article
- 1985
-
Mark
Recurrent otitis media : genetic immunoglobulin markers in children and their parents
(
- Contribution to journal › Article