Novel interstitial 2.6 Mb deletion on 9q21 associated with multiple congenital anomalies-Reference-Cited by-同舟云学术

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Novel interstitial 2.6 Mb deletion on 9q21 associated with multiple congenital anomalies

Published:2013-11-25 Issue:1 Volume:164 Page:237-242
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Pua Heather H.¹,Krishnamurthi Swetha²,Farrell Jessica¹,Margeta Marta¹,Ursell Philip C.¹,Powers Martin¹³,Slavotinek Anne M.²,Jeng Linda J.B.³

Affiliation:

1. Department of Pathology; University of California San Francisco; San Francisco California

2. Division of Genetics; Department of Pediatrics; University of California San Francisco; San Francisco California

3. Department of Laboratory Medicine; University of California San Francisco; San Francisco California

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36230/fullpdf

Reference27 articles.

1. Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21;Allen-Brady;Am J Hum Genet,2009

2. Sequence analysis of the GntII (subsidiary) system for gluconate metabolism reveals a novel pathway for L-idonic acid catabolism in Escherichia coli;Bausch;J Bacteriol,1998

3. hnRNP K: One protein multiple processes;Bomsztyk;BioEssays,2004

4. Identification of PRTFDC1 silencing and aberrant promter methylation of GPR150, ITGA8, and HOXD11 in ovarian cancers;Cai;Life Sci,2007

5. Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency;Chen;Prenat Diagn,2005

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