Document Detail


Consideration of VACTERL association in patients with trisomy 21.
MedLine Citation:
PMID:  20512033     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Authors:
Benjamin D Solomon; Sophia M Bous; Simona Bianconi; Daniel E Pineda-Alvarez
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, N.I.H., Intramural    
Journal Detail:
Title:  Clinical dysmorphology     Volume:  19     ISSN:  1473-5717     ISO Abbreviation:  Clin. Dysmorphol.     Publication Date:  2010 Oct 
Date Detail:
Created Date:  2010-09-08     Completed Date:  2011-01-03     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  9207893     Medline TA:  Clin Dysmorphol     Country:  England    
Other Details:
Languages:  eng     Pagination:  209-11     Citation Subset:  IM    
Affiliation:
Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA. solomonb@mail.nih.gov
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Anal Canal / abnormalities
Down Syndrome*
Esophagus / abnormalities
Female
Heart Defects, Congenital* / genetics
Humans
Infant
Kidney / abnormalities
Limb Deformities, Congenital* / genetics
Spine / abnormalities
Trachea / abnormalities
Comments/Corrections

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


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