Phenotype and 244k array-CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1-qter-Reference-Cited by-同舟云学术

Phenotype and 244k array-CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1-qter

Published:2009-04-10 Issue:5 Volume:149A Page:894-905
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kirchhoff Maria,Bisgaard Anne-Marie,Stoeva Radka,Dimitrov Boyan,Gillessen-Kaesbach Gabriele,Fryns Jean-Pierre,Rose Hanne,Grozdanova Liliana,Ivanov Ivan,Keymolen Kathelijn,Fagerberg Christina,Tranebjaerg Lisbeth,Skovby Flemming,Stefanova Margarita

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32814/fullpdf

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3. 13q 2007. Deletion and central nervous system anomalies: Further insights from karyotype-phenotype analyses of 14 patients;Ballarati;J Med Genet,2007

4. Evidence for a critical region for penoscrotal inversion, hypospadias, and imperforate anus within chromosomal region 13q32.2q34;Bartsch;Am J Med Genet,1996

5. Cloning and characterization of a novel beta integrin-related cDNA coding for the protein TIED (“ten beta integrin EGF-like repeat domains”) that maps to chromosome band 13q33: A divergent stand-alone integrin stalk structure;Berg;Genomics,1999

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