CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS
Muzammil Ahmad Khan
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Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis [PDF]
Pascal Lefèvre +7 more
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Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
Yunqing Ren +8 more
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Hypotrichosis and Hair Loss on the Occipital Scalp [PDF]
Erica Possa de Abreu
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Management of hypotrichosis of the eyelashes: Focus on bimatoprost
Steven Fagien
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Correction: Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report [PDF]
Giovanna Carnovale-Scalzo +9 more
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Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population. [PDF]
Somani V, Somani A, Annabathula A.
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Mutations in Lipase H Gene Underlie Autosomal Recessive Hypotrichosis in Five Pakistani Families
U.‐E Kalsoom +6 more
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Exome sequencing reveals mutation inGJA1as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome [PDF]
Huijun Wang +16 more
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