Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: Delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications-Reference-Cited by-同舟云学术

Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: Delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications

Published:2005 Issue:2 Volume:138A Page:175-180
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Yatsenko Svetlana A.,Treadwell-Deering Diane,Krull Kevin,Lewis Richard Alan,Glaze Daniel,Stankiewicz Pawel,Lupski James R.,Potocki Lorraine

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats

2. Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse

3. Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2

4. Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

5. CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature

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