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hypotrichosis localized
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OMIM - Skin Related Disorders
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A novel mutation in lysophosphatidic acid receptor 6 gene in autosomal recessive hypotrichosis and e…
A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair.
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Easte…
Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosoma…
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Efficacy of Topical Gentamycin for Hereditary Hypotrichosis Simplex Caused by Nonsense Mutations in …
Safety and Patient Satisfaction With GLASH VISTA™ (Bimatoprost 0.03%) in the Treatment of Eyelash Hy…
Dutasteride Versus Placebo and Finasteride in Men With Androgenetic Alopecia
Intraamniotic Administrations of ER004 to Male Subjects With X-linked Hypohidrotic Ectodermal Dyspla…
A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) in Combination With Ribavirin in Patients With Chr…
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