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Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani familiesTARIQ, M; AYUB, M; YASINZAI, M et al.British journal of dermatology (1951). 2009, Vol 160, Num 5, pp 1006-1010, issn 0007-0963, 5 p.Article

A rare cause of syndromic hypotrichosis : Nicolaides-Baraitser syndromeCASTORI, Marco; COVACIU, Claudia; RINALDI, Rosanna et al.Journal of the American Academy of Dermatology. 2008, Vol 59, Num 5, issn 0190-9622, S92-S98, SUPArticle

THREE VARIATIONS OF HAIRLESSNESS ASSOCIATED WITH ALBINISM IN THE LABORATORY RATFERGUSON FG; IRVING GW III; STEDHAM MA et al.1979; LAB. ANIMAL SCI.; USA; DA. 1979; VOL. 29; NO 4; PP. 459-465; BIBL. 12 REF.Article

DISORDERS OF THE HAIR IN CHILDREN.PRICE VH.1978; PEDIATR. CLIN. N. AMER.; USA; DA. 1978; VOL. 25; NO 2; PP. 305-320; BIBL. 41 REF.Article

Autosomal recessive ichthyosis with hypotrichosis syndrome : further delineation of the phenotypeAVRAHAMI, L; MAAS, S; PASMANIK-CHOR, M et al.Clinical genetics. 2008, Vol 74, Num 1, pp 47-53, issn 0009-9163, 7 p.Article

Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32WALI, A; CHISHTI, M. S; AYUB, M et al.Clinical genetics. 2007, Vol 72, Num 1, pp 23-29, issn 0009-9163, 7 p.Article

Nevus psiloliparus: Report of two nonsyndromic casesHAPPLE, Rudolf; HÖRSTER, Stefan.EJD. European journal of dermatology. 2004, Vol 14, Num 5, pp 314-316, issn 1167-1122, 3 p.Article

Focal naevoid hypotrichosisBARTH, J. H; DAWBER, R. P. R.Acta dermato-venereologica. 1987, Vol 67, Num 2, pp 178-179, issn 0001-5555Article

Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hairPASTERNACK, Sandra M; MURUGUSUNDRAM, Sundaram; EIGELSHOVEN, Sibylle et al.Archives of dermatological research (Print). 2009, Vol 301, Num 8, pp 621-624, issn 0340-3696, 4 p.Article

Histopathology of hypotrichosis with juvenile macular dystrophyBERGMAN, Reuven; SAPIR, Marcela; SPRECHER, Eli et al.The American journal of dermatopathology. 2004, Vol 26, Num 3, pp 205-209, issn 0193-1091, 5 p.Article

A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophyINDELMAN, Margarita; BERGMAN, Reuven; LURIE, Raziel et al.Journal of investigative dermatology. 2002, Vol 119, Num 5, pp 1210-1213, issn 0022-202X, 4 p.Article

ALOFACIE ET HYPOTRICHOSE CONGENITALESKHALILOVA IM; AVANESOV AA; GANIEV KD et al.1977; VEST. DERMATOL. VENEROL.; S.S.S.R.; DA. 1977; NO 8; PP. 66-68; ABS. ANGL.; BIBL. DISSEM.Article

Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophyINDELMAN, Margarita; HAMEL, Christian P; LURIE, Raziel et al.Journal of investigative dermatology. 2003, Vol 121, Num 5, pp 1217-1220, issn 0022-202X, 4 p.Article

STRUCTURAL HAIR ABNORMALITIES IN HIDROTIC ECTODERMAL DYSPLASIA (HED).WILSCH L; HANEKE E; SCHAIDI G et al.1977; ARCH. DERMATOL. RES.; GERM.; DA. 1977; VOL. 259; NO 1; PP. 101-103; BIBL. 4 REF.Article

HIDROTIC ECTODERMAL DYSPLASIA IN A BLACK MOTHER AND DAUGHTER.MCNAUGHTON PZ; PIERSON DL; RODMAN OG et al.1976; ARCH. DERMATOL.; U.S.A.; DA. 1976; VOL. 112; NO 10; PP. 1448-1450; BIBL. 5 REF.Article

STEATOCYSTOMA MULTIPLEX.COLE LA.1976; ARCH. DERMATOL.; U.S.A.; DA. 1976; VOL. 112; NO 10; PP. 1437-1439; BIBL. 24 REF.Article

A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2). DiscussionKAMRAN-UL-HASSAN NAQVI, S; RAZA, S. I; NAVEED, A. K et al.British journal of dermatology (1951). 2009, Vol 160, Num 1, pp 194-196, issn 0007-0963, 3 p.Article

Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23―22.3NAZ, Gul; ALI, Ghazanfar; SYED KAMRAN-UL-HASSAN NAQVI et al.Human genetics. 2010, Vol 127, Num 4, pp 395-401, issn 0340-6717, 7 p.Article

Hypotrichose héréditaire de Marie Unna = Hereditary hypotrichosis Marie Unna TypeLALEVIC-VASIC, B. M; POLIC, D; NIKOLIC, M. M et al.Annales de dermatologie et de vénéréologie. 1992, Vol 119, Num 1, pp 25-29, issn 0151-9638Article

Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular DystrophyHALFORD, Stephanie; HOLT, Richard; NEMETH, Andrea H et al.Archives of ophthalmology (1960). 2012, Vol 130, Num 11, pp 1490-1492, issn 0003-9950, 3 p.Article

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYARAN WEN; YANG LIU; KRUSE, Roland et al.Nature genetics. 2009, Vol 41, Num 2, pp 228-233, issn 1061-4036, 6 p.Article

Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophyINDELMAN, M; EASON, J; HUMMEL, M et al.Clinical and experimental dermatology (Print). 2007, Vol 32, Num 2, pp 191-196, issn 0307-6938, 6 p.Article

Hereditary hypotrichosis simplex of the scalpKOHN, G; METZKER, A.Clinical genetics. 1987, Vol 32, Num 2, pp 120-124, issn 0009-9163Article

Hypotrichosis congenita hereditaria Marie Unna = Hypotrichose congénitale héréditaire de Marie UnnaWIRTH, G; BINDEWALD, I; KÜSTER, W et al.Hautarzt. 1985, Vol 36, Num 10, pp 577-580, issn 0017-8470Article

A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/HypotrichosisFUJIMOTO, Atsushi; FAROOQ, Muhammad; ITO, Masaaki et al.Journal of investigative dermatology. 2012, Vol 132, Num 10, pp 2342-2349, issn 0022-202X, 8 p.Article

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