9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism-Reference-Cited by-同舟云学术

9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism

Published:2013-07-03 Issue:8 Volume:161 Page:1882-1896
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Quinonez Shane C.¹,Park John M.²,Rabah Raja³,Owens Kailey M.¹,Yashar Beverly M.⁴,Glover Thomas W.,Keegan Catherine E.

Affiliation:

1. Department of Pediatrics, Division of Genetics; University of Michigan; Ann Arbor; Michigan

2. Department of Urology; University of Michigan; Ann Arbor; Michigan

3. Department of Pathology; University of Michigan; Ann Arbor; Michigan

4. Department of Human Genetics; University of Michigan; Ann Arbor; Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36018/fullpdf

Reference111 articles.

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2. Deletion of the short arm of chromosome #9 (46,9p-): A new deletion syndrome;Alfi;Ann Génét,1973

3. The 9p- syndrome;Alfi;Ann Génét,1976

4. A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardation;Argyriou;Clin Dysmorphol,2010

5. De novo duplication of 7pter->p21.2 and deletion of 9pter->p23.5: Clinical and cytogenetic diagnosis;Back;Clin Genet,1997

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