1 – 50 of 50
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark
(
- Contribution to journal › Article
- 2020
-
Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
(
- Contribution to journal › Article
- 2019
-
Mark
Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy
(
- Contribution to journal › Article
- 2015
-
Mark
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation
(
- Contribution to journal › Article
- 2014
-
Mark
Intralocus sexual conflict over wing length in a wild migratory bird
(
- Contribution to journal › Article
- 2013
-
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
Rare allelic forms of PRDM9 associated with childhood leukemogenesis
(
- Contribution to journal › Article
- 2011
-
Mark
Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene
(
- Contribution to journal › Article
- 2009
-
Mark
Familial associations of rheumatoid arthritis with autoimmune diseases and related conditions
(
- Contribution to journal › Article
- 2008
-
Mark
The effect of pedigree structure on detection of deletions and other null alleles.
(
- Contribution to journal › Article
-
Mark
Concordance of survival in family members with prostate cancer
(
- Contribution to journal › Article
- 2007
-
Mark
Vägen till vinnarcirkeln. Travhästen och dess människor mellan sport och spel
2007)(
- Thesis › Doctoral thesis (monograph)
-
Mark
Detecting Deletions by Analysis of Genetic Markers in Pedigrees
2007)(
- Thesis › Doctoral thesis (compilation)
-
Mark
No evidence for inbreeding avoidance in a great reed warbler population
(
- Contribution to journal › Article
- 2006
-
Mark
Familial risks of aortic aneurysms among siblings in a nationwide Swedish study
(
- Contribution to journal › Article
- 2005
-
Mark
Familial multiple primary lung cancers : a population-based analysis from Sweden
(
- Contribution to journal › Article
- 2004
-
Mark
BRCA1 och BRCA2 har nått kliniken. Tioårigt fynd av genmutation ger nu möjlighet förebygga ärftlig bröstcan
(
- Contribution to journal › Article
-
Mark
Association of brain tumours with other neoplasms in families
(
- Contribution to journal › Article
-
Mark
Familial aggregation of Hodgkin lymphoma and related tumors
(
- Contribution to journal › Article
- 2003
-
Mark
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
(
- Contribution to journal › Article
-
Mark
Familial risks in nervous system tumors
2003) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 12(11 Pt 1). p.1137-1142(
- Contribution to journal › Article
-
Mark
Familial risk of cancer by site and histopathology
(
- Contribution to journal › Article
- 2002
-
Mark
Analysis of atrioventricular plane movements by Doppler tissue imaging and m-mode in children with atrial septal defects before and after surgical and device closure.
(
- Contribution to journal › Article
-
Mark
Coil embolization of a neonatal pulmonary arteriovenous malformation.
(
- Contribution to journal › Article
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity.
(
- Contribution to journal › Article
-
Mark
Cancer risks in Nordic immigrants and their offspring in Sweden
(
- Contribution to journal › Article
- 2001
-
Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
(
- Contribution to journal › Article
-
Mark
The nation-wide Swedish family-cancer database--updated structure and familial rates
(
- Contribution to journal › Article
-
Mark
A population-based study of familial central nervous system hemangioblastomas
(
- Contribution to journal › Article
-
Mark
Second primary cancers after sporadic and familial colorectal cancer
2001) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 10(7). p.8-793(
- Contribution to journal › Article
-
Mark
Parental cancer as a risk factor for brain tumors (Sweden)
(
- Contribution to journal › Article
-
Mark
A population-based study of familial soft tissue tumors
(
- Contribution to journal › Article
- 2000
-
Mark
Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation
(
- Contribution to journal › Article
-
Mark
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
(
- Contribution to journal › Article
-
Mark
Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer
(
- Contribution to journal › Article
- 1999
-
Mark
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study
(
- Contribution to journal › Article
- 1998
-
Mark
BRCA1-positive patients are small for gestational age compared with their unaffected relatives
(
- Contribution to journal › Article
- 1997
-
Mark
von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura
(
- Contribution to journal › Article
-
Mark
The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer : a population-based cohort study
(
- Contribution to journal › Article
-
Mark
A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction
(
- Contribution to journal › Article
- 1996
-
Mark
A novel p53 germline alteration identified in a late onset breast cancer kindred
(
- Contribution to journal › Article
-
Mark
Novel germline p16 mutation in familial malignant melanoma in southern Sweden
(
- Contribution to journal › Article
-
Mark
Familial testicular cancer in Norway and southern Sweden
(
- Contribution to journal › Article
- 1993
-
Mark
Haemophilia : strategies for carrier detection and prenatal diagnosis
(
- Contribution to journal › Article
- 1990
-
Mark
Two factor IX mutations in the family of an isolated haemophilia B patient : direct carrier diagnosis by amplification mismatch detection (AMD)
(
- Contribution to journal › Article
- 1987
-
Mark
Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage
(
- Contribution to journal › Article
- 1982
-
Mark
Genetic variants of haemophilia B detected by immunoradiometric assay : implications for prenatal diagnosis
(
- Contribution to journal › Article
- 1981
-
Mark
Inheritable molecular variants of moderate and mild hemophilia A
(
- Contribution to journal › Article