Myelodysplastic syndrome in a kindred with ins(16) (p11.2)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb03474.x/fullpdf
Reference15 articles.
1. Proposals for the classification of the myelodysplastic syndromes;Bennett;Br. J. Haematol.,1982
2. Report of the committee on the genetic constitution of chromosomes 13, 14, 15 and 16;Cox;Cytogenet. Cell Genet.,1985
3. Polymorphism of human constitutive heterochromatin;Craig-Holmes;Science,1971
4. Abnormality of chromosome 16 and its phenotypic expression;Golden;Clin. Genet.,1981
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2. Constitutional chromosome aberrations as pathogenetic events in hematologic malignancies;Cancer Genetics and Cytogenetics;2004-03
3. Prenatal diagnosis of dichromatic 16p+ heteromorphisms in two unrelated families;Prenatal Diagnosis;1991-06
4. Euchromatic 16p + heteromorphism: First report in North America;American Journal of Medical Genetics;1990-12
5. Clonal karyotype abnormalities and clinical progress in the myelodysplastic syndrome;British Journal of Haematology;1990-10
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