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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2003-3-25
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pubmed:databankReference |
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pubmed:abstractText |
Congenital atrichias represent a complex and heterogeneous group of genodermatoses, which have been shown in several consanguineous families to result from homozygous mutations in the hairless gene (HR).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0007-0963
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
148
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
553-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12653749-Alopecia,
pubmed-meshheading:12653749-Child, Preschool,
pubmed-meshheading:12653749-DNA Mutational Analysis,
pubmed-meshheading:12653749-Female,
pubmed-meshheading:12653749-Gene Deletion,
pubmed-meshheading:12653749-Heterozygote Detection,
pubmed-meshheading:12653749-Humans,
pubmed-meshheading:12653749-Infant,
pubmed-meshheading:12653749-Male,
pubmed-meshheading:12653749-Microsatellite Repeats,
pubmed-meshheading:12653749-Pedigree,
pubmed-meshheading:12653749-Polymerase Chain Reaction
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pubmed:year |
2003
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pubmed:articleTitle |
Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesions.
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pubmed:affiliation |
Department of Dermatology and Laboratory of Molecular Dermatology, Rambam Medical Center, Haifa, Israel.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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