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8162159
Source:
http://linkedlifedata.com/resource/pubmed/id/8162159
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41
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017431
,
umls-concept:C0031437
,
umls-concept:C0033053
,
umls-concept:C0039585
,
umls-concept:C0392360
,
umls-concept:C1850620
pubmed:issue
4
pubmed:dateCreated
1994-5-24
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8162159-7909256
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9423848
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0804-4643
pubmed:author
pubmed-author:ForestM GMG
,
pubmed-author:MebarkiFF
,
pubmed-author:MonárSS
pubmed:issnType
Print
pubmed:volume
130
pubmed:geneSymbol
AR
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
325-6
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:8162159-Androgen-Insensitivity Syndrome
,
pubmed-meshheading:8162159-Female
,
pubmed-meshheading:8162159-Fetal Diseases
,
pubmed-meshheading:8162159-Genotype
,
pubmed-meshheading:8162159-Humans
,
pubmed-meshheading:8162159-Male
,
pubmed-meshheading:8162159-Phenotype
,
pubmed-meshheading:8162159-Point Mutation
,
pubmed-meshheading:8162159-Pregnancy
,
pubmed-meshheading:8162159-Prenatal Diagnosis
pubmed:year
1994
pubmed:articleTitle
What are the indications for prenatal diagnosis in the androgen insensitivity syndrome? Facing clinical heterogeneity of phenotypes for the same genotype.
pubmed:affiliation
INSERM U329, Laboratoire de Biochimie endocrinienne et moléculaire, Hôpital Debrousse, Lyon, France.
pubmed:publicationType
Journal Article
,
Comment