Document Detail


Array CGH ends diagnostic odyssey for infant with features of Williams and Alagille syndrome.
MedLine Citation:
PMID:  19396828     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Authors:
C Honeywell; L Gardin; C Jimenez-Rivera; J Allanson
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Publication Detail:
Type:  Comment; Letter    
Journal Detail:
Title:  American journal of medical genetics. Part A     Volume:  149A     ISSN:  1552-4833     ISO Abbreviation:  Am. J. Med. Genet. A     Publication Date:  2009 May 
Date Detail:
Created Date:  2009-05-04     Completed Date:  2009-06-18     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101235741     Medline TA:  Am J Med Genet A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1102-3     Citation Subset:  IM    
Export Citation:
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MeSH Terms
Descriptor/Qualifier:
Alagille Syndrome / diagnosis*
Comparative Genomic Hybridization
Humans
Infant
Oligonucleotide Array Sequence Analysis
Williams Syndrome / diagnosis*
Comments/Corrections
Comment On:
Am J Med Genet A. 2008 Sep 15;146A(18):2407-11   [PMID:  18688871 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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