Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints-Reference-Cited by-同舟云学术

Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints

Published:2010-11-24 Issue:12 Volume:152A Page:3074-3083
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gajecka Marzena,Saitta Sulagna C.,Gentles Andrew J.,Campbell Lindsey,Ciprero Karen,Geiger Elizabeth,Catherwood Anne,Rosenfeld Jill A.,Shaikh Tamim,Shaffer Lisa G.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33733/fullpdf

Reference42 articles.

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4. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication;Ballif;Mol Cytogenet,2008a

5. Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2;Ballif;Clin Genet,2008b

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