Hypotrichosis: New Insights for the Healthcare Professional: 2011 Edition: ScholarlyPaper
ScholarlyEditions, Jan 9, 2012 - Medical - 16 pages
Hypotrichosis: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Hypotrichosis in a compact format.
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Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis
Splice site mutations in the Pcadherin gene underlie hypotrichosis with juvenile macular dystrophy
Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
Bile duct paucity is part of the neonatal ichthyosissclerosing cholangitis phenotype
A homozygous nonsense mutation in the human desmocollin3 DSC3 gene underlies hereditary hypotrichosis and recurrent skin vesicles
Genetic mapping of a novel hypotrichosis locus to chromosome 7p213p223 in a Pakistani family and screening of the candidate genes
A new locus for hereditary hypotrichosis simplex maps to chromosome 13q1212 approximately 123 in a Chinese family