Division of Clinical Genetics
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- 2002
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Mark
Congenital and inherited syndromes associated with bone and soft tissue tumours
2002) p.349-349(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Chordoma
2002) p.316-316(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Synovial chondromatosis
2002) p.246-246(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Coping with complexity. multivariate analysis of tumor karyotypes.
(
- Contribution to journal › Article
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Mark
SYT-SSX is critical for cyclin D1 expression in synovial sarcoma cells: A gain of function of the t(X;18)(p11.2;q11.2) translocation
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- Contribution to journal › Article
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Mark
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck.
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- Contribution to journal › Article
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Mark
Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
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- Contribution to journal › Article
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Mark
Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer.
(
- Contribution to journal › Article
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Mark
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
(
- Contribution to journal › Article
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Mark
Solid tumor cytogenetics
2002) p.704-704(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Clonal chromosome abnormalities in premalignant lesions of the skin.
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- Contribution to journal › Article
- 2001
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Mark
Issues in Human GenEthics
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- Contribution to journal › Article
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Mark
Cloning of the der(17)t(X;17)(p11;q25) alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
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Mark
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder
(
- Contribution to journal › Published meeting abstract
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Mark
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
(
- Contribution to journal › Article
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Mark
Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping
(
- Contribution to journal › Article
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Mark
Involvement and intrinsic deficiencies of hematopoietic stem cells in MDS patients with trisomy 8
(
- Contribution to journal › Article
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Mark
Essential genetics education for non-genetics health professionals (EC Project GenEd)
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- Contribution to journal › Article
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Mark
Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and fish analysis
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- Contribution to journal › Article
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Mark
Trisomy 7 accumulates with age in solid tumors and non-neoplastic synovia
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- Contribution to journal › Article
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Mark
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone
(
- Contribution to journal › Article
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Mark
Smoking and acute myeloid leukemia: associations with morphology and karyotypic patterns and evaluation of dose-response relations
2001) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis 25(10). p.865-872(
- Contribution to journal › Article
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Mark
Isodicentric 7p, idic(7)(q11.2), in acute myeloid
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- Contribution to journal › Article
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Mark
Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors
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- Contribution to journal › Article
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Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
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- Contribution to journal › Article
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Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
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- Contribution to journal › Article
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Mark
Distinct cytologic features of spindle cell lipoma - A cytologic-histologic study with clinical, radiologic, electron microscopic, and cytogenetic correlations
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- Contribution to journal › Article
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Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
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- Contribution to journal › Article
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Mark
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
(
- Contribution to journal › Article
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Mark
Comparative genomic hybridization of postirradiation sarcomas
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- Contribution to journal › Article
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Mark
The absence of high-frequency QRS changes in the presence of standard electrocardiographic QRS changes of old myocardial infarction
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- Contribution to journal › Article
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Mark
Abnormal nuclear shape in solid tumors reflects mitotic instability
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- Contribution to journal › Article
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Mark
Clinical impact of molecular and cytogenetic findings in synovial sarcoma
(
- Contribution to journal › Article
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Mark
Proliferation of primitive myeloid progenitors can be reversibly induced by HOXA10
(
- Contribution to journal › Article
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Mark
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
(
- Contribution to journal › Article
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Mark
ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization
(
- Contribution to journal › Article
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Mark
Paired multiplex reverse-transcriptase polymerase chain reaction (PMRT-PCR) analysis as a rapid and accurate diagnostic tool for the detection of MLL fusion genes in hematologic malignancies
(
- Contribution to journal › Article
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Mark
Refined characterisation of chromosome aberrations in tumours by multicolour banding and electronic mapping resources
2001) In Methods in cell science: an official journal of the Society for In Vitro Biology 23(1-3). p.23-28(
- Contribution to journal › Article
-
Mark
The tumor-associated gene HMGIC is expressed in normal and osteoarthritis-affected synovia
(
- Contribution to journal › Article
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Mark
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology
(
- Contribution to journal › Article
-
Mark
Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
-
Mark
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis
(
- Contribution to journal › Article
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Mark
Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia?
(
- Contribution to journal › Article
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Mark
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer
(
- Contribution to journal › Article
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Mark
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex
(
- Contribution to journal › Article
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Mark
Limitations of chromosome classification by multicolor karyotyping
(
- Contribution to journal › Article
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Mark
Identification of human candidate genes for male infertility by digital differential display
(
- Contribution to journal › Article
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Mark
PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms
(
- Contribution to journal › Article
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Mark
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
(
- Contribution to journal › Article
-
Mark
Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: Diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years
(
- Contribution to journal › Article