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11069461
Source:
http://linkedlifedata.com/resource/pubmed/id/11069461
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48
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Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0015576
,
umls-concept:C0017337
,
umls-concept:C0439660
,
umls-concept:C0796348
,
umls-concept:C1556085
,
umls-concept:C1708726
,
umls-concept:C2931059
pubmed:issue
4
pubmed:dateCreated
2000-11-20
pubmed:abstractText
Hypotrichosis of the Marie Unna type (HMU) is a rare autosomal dominant disorder characterized by male-pattern hair loss with childhood onset and anomalies of the hair shaft.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0004041
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0007-0963
pubmed:author
pubmed-author:AltlandKK
,
pubmed-author:AnkerMM
,
pubmed-author:CichonSS
,
pubmed-author:HillmerA MAM
,
pubmed-author:KnappMM
,
pubmed-author:KukukGG
,
pubmed-author:LVOVAT NTN
,
pubmed-author:NöthenM MMM
,
pubmed-author:ProppingPP
pubmed:issnType
Print
pubmed:volume
143
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
811-4
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11069461-Adult
,
pubmed-meshheading:11069461-Chromosome Mapping
,
pubmed-meshheading:11069461-Chromosomes, Human, Pair 8
,
pubmed-meshheading:11069461-DNA Mutational Analysis
,
pubmed-meshheading:11069461-Female
,
pubmed-meshheading:11069461-Humans
,
pubmed-meshheading:11069461-Hypotrichosis
,
pubmed-meshheading:11069461-Lod Score
,
pubmed-meshheading:11069461-Male
,
pubmed-meshheading:11069461-Microsatellite Repeats
,
pubmed-meshheading:11069461-Pedigree
pubmed:year
2000
pubmed:articleTitle
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
pubmed:affiliation
Institute of Human Genetics, University of Bonn, Wilhelmstr. 31, 53111 Bonn, Germany. cichon@mailer.meb.uni-bonn.de
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't