A novel mutation in Lysophosphatidic Acid Receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effectAZHAR, Aysha; TARIQ, Muhammad; MAHMOOD BAIG, Shahid et al.EJD. European journal of dermatology. 2012, Vol 22, Num 4, pp 464-466, issn 1167-1122, 3 p.Article

Marie Unna Hereditary Hypotrichosis: A Turkish Family With Loss of Eyebrows and a U2HR MutationMANSUR, Ayse Tulin; ELCIOGLU, Nursel H; REDLER, Silke et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 10, pp 2628-2633, issn 1552-4825, 6 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

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

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

Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hairMAHMOUDI, Hassnaa; TUG, Esra; HAYDAR PARLAK, Ali et al.Experimental dermatology. 2012, Vol 21, Num 6, pp 469-471, issn 0906-6705, 3 p.Article

A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2)JELANI, M; WASIF, N; ALI, G et al.Clinical genetics. 2008, Vol 74, Num 2, pp 184-188, issn 0009-9163, 5 p.Article

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

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

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

Light and scanning electron microscopic examination of late changes in hair with hereditary trichodysplasia (Marie Unna hypotrichosis)CELIK, Hamdi H; SURUCU, Selcuk H; ALDUR, Mustafa M et al.Saudi medical journal. 2004, Vol 25, Num 11, pp 1648-1651, issn 0379-5284, 4 p.Article

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherinSPRECHER, Eli; BERGMAN, Reuven; COHEN, Nadine et al.Nature genetics. 2001, Vol 29, Num 2, pp 134-136, issn 1061-4036Article

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

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

Identification of a novel U2HR mutation c.14C>T in a Chinese patient with Marie Unna hereditary hypotrichosisZHOU, Cheng; ZANG, Dongjie; MA, Xiaolei et al.EJD. European journal of dermatology. 2012, Vol 22, Num 1, pp 34-35, issn 1167-1122, 2 p.Article

Identification of a novel locus for marie unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3SEN YANG; MIN GAO; SUN, Liang-Dan et al.Journal of investigative dermatology. 2005, Vol 125, Num 4, pp 711-714, issn 0022-202X, 4 p.Article

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3HE, P. P; ZHANG, X. J; SUN, L. D et al.British journal of dermatology (1951). 2004, Vol 150, Num 5, pp 837-842, issn 0007-0963, 6 p.Article

Hypotrichosis with juvenile macular dystrophy : Clinical and electrophysiological assessment of visual functionLEIBU, Rina; JERMANS, Anna; HATIM, Ghantus et al.Ophthalmology (Rochester, MN). 2006, Vol 113, Num 5, pp 841-847, issn 0161-6420, 7 p.Article

A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalpNAHUM, S; MORICE-PICARD, F; TAIEB, A et al.Clinical and experimental dermatology (Print). 2011, Vol 36, Num 2, pp 188-194, issn 0307-6938, 7 p.Article

Mutations homozygotes non-sens du gène de la desmocolline-3 et hypotrichose avec vésicules récidivantes = Homozygous nonsense mutations in the desmocollin-3 gene and hypotrichosis with recurrent vesiclesDEREURE, O.Annales de dermatologie et de vénéréologie. 2010, Vol 137, Num 6-7, issn 0151-9638, p. 495Article

Hypotrichosis, Bulbous Nose, and Cone-Shaped Epiphyses in an 8-Year-Old GirlSAYED, Christopher J; MATHEIS, Patricia; MORRELL, Dean S et al.Pediatric dermatology. 2008, Vol 25, Num 5, pp 557-558, issn 0736-8046, 1 p.Article