Microarray based analysis of 3p25-p26 deletions (3p- syndrome)-Reference-Cited by-同舟云学术

Microarray based analysis of 3p25-p26 deletions (3p- syndrome)

Published:2009-10 Issue:10 Volume:149A Page:2099-2105
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shuib Salwati,McMullan Dominic,Rattenberry Eleanor,Barber Richard M.,Rahman Fatimah,Zatyka Malgosia,Chapman Cyril,Macdonald Fiona,Latif Farida,Davison Val,Maher Eamonn R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference39 articles.

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2. Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2;Ballif;Nat Genet,2007

3. Terminal 3p deletions: Phenotypic variability, chromosomal non-penetrance or gene modification?;Barber;Am Med Genet Part A,2008

4. 46, XY, del (3) (pter → p25) syndrome: Further delineation of the clinical phenotype;Benini;Eur J Pediatr,1999

5. Molecular cytogenetic characterization of a subtle interstitial del (3)(p25.3p26.2) in a patient with deletion 3p syndrome;Cargile;Am J Med Genet,2002

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