Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter-Reference-Cited by-同舟云学术

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Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter

Published:2005 Issue:1 Volume:136A Page:38-44
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Archer H.L.,Gupta S.,Enoch S.,Thompson P.,Rowbottom A.,Chua I.,Warren S.,Johnson D.,Ledbetter D.H.,Lese-Martin C.,Williams P.,Pilz D.T.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference47 articles.

1. Cloning, Chromosal Mapping, and Tissue Expression of the Gene Encoding the Human Eph-Family Kinase Ligand Ephrin-A2

2. The end of the beginning of chromosome ends

3. Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13.3

4. Telomeres: a diagnosis at the end of the chromosomes

5. BMP signaling is required for septation of the outflow tract of the mammalian heart

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4. A case with cardiac, skeletal, speech, and motor traits narrows the subtelomeric 19p13.3 microdeletion region to 46 kb;American Journal of Medical Genetics Part A;2022-10-22

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