Document Detail


Ambral syndrome and congenital generalized hypertrichosis.
MedLine Citation:
PMID:  7889653     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Authors:
L E Figuera; J M Cantu
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Publication Detail:
Type:  Comment; Letter    
Journal Detail:
Title:  Clinical genetics     Volume:  46     ISSN:  0009-9163     ISO Abbreviation:  Clin. Genet.     Publication Date:  1994 Nov 
Date Detail:
Created Date:  1995-04-18     Completed Date:  1995-04-18     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0253664     Medline TA:  Clin Genet     Country:  DENMARK    
Other Details:
Languages:  eng     Pagination:  384     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Chromosome Aberrations*
Chromosome Disorders*
Chromosomes, Human, Pair 8* / genetics
Female
Humans
Hypertrichosis / congenital*
Male
Syndrome
Comments/Corrections
Comment On:
Clin Genet. 1993 Sep;44(3):121-8   [PMID:  8275569 ]

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


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