Velocardiofacial syndrome with a rare t(2;22)-Reference-Cited by-同舟云学术

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Velocardiofacial syndrome with a rare t(2;22)

Published:2007-07 Issue:3 Volume:16 Page:181-183
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Huber Jair,Rainho Claudia A.,Gomes Marcus V.,Santos Silvio A.,Ramos Ester S.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals;Casas;Am J Med Genet,2004

2. Fragile sites and structural rearrangements in cancer;De Braekeleer;Hum Genet,1985

3. A-T rich palindromes mediate the constitutional t(11,22) translocation;Edelmann;Am J Hum Genet,2001

4. Chromosomes and causation of human cancer and leukemia. XVI. Banding studies of chronic myelocytic leukemia, including five unusual Ph11 translocations;Hayata;Cancer,1975

5. Cytogenetic peculiarities in chronic myelogenous leukemia;Hild;Cancer Genet Cytogenet,1990

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