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

Alopécie totale chez deux sœurs = Alopecia totalis in two sistersREYGAGNE, P.Images en dermatologie. 2012, Vol 5, Num 6, pp 144-147, issn 1964-4167, 4 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

SEUIL DE PENETRANCE ET EXPRESSIVITE D'UN GENE RECESSIF: CAS DE L'HYPOTRICHOSE PERIODIQUE CHEZ LA SOURISKOBOZIEFF N; LUCOTTE G; GEMAHLING E et al.1974; EXPER. ANIMALE; FR.; DA. 1974; VOL. 7; NO 4; PP. 163-172; BIBL. 13REF.Article

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

The gene for hypotrichosis of Marie Unna maps between D8S258 and d8S298 : Exclusion of the hr gene by cDNA and genomic sequencingVAN STEENSEL, M; SMITH, F. J. D; DOHERTY, V. R et al.American journal of human genetics. 1999, Vol 65, Num 2, pp 413-419, issn 0002-9297Article

Des cheveux cassants = Broken hairMAZEREEUW-HAUTIER, J.Images en dermatologie. 2012, Vol 5, Num 6, pp 118-119, issn 1964-4167, 2 p.Article

La dysplasie ectodermique anhydrotique : présentation de quatre observations = Anhidrotic ectomermal dysplasia (AED) : four casesSOUBEYRAND, E; NICOLAS, J; LABBE, D et al.Revue de stomatologie et de chirurgie maxillo-faciale. 2005, Vol 106, Num 6, pp 328-333, issn 0035-1768, 6 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

HEREDITARY HYPOTRICHOSIS SIMPLEX OF THE SCALP. EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCE = HYPOTRICHOSE HEREDITAIRE DU CUIR CHEVELU. MISE EN EVIDENCE DE LA TRANSMISSION SUR LE MODE AUTOSOMAL DOMINANTTORIBIO J; QUINONES PA.1974; BRIT. J. DERMATOL.; G.B.; DA. 1974; VOL. 91; NO 6; PP. 687-696; BIBL. 9 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

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

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

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

Hair restoration surgery in patients with hypotrichosis of the pubis : The reason and ideas for design. CommentaryCHANG KWUN HONG; HAN GYU CHOI; SWINEHART, J. M et al.Dermatologic surgery. 1999, Vol 25, Num 6, pp 475-479, issn 1076-0512Article

Hypotrichosis congenita hereditaria Marie Unna = Hypotrichose congénitale héréditaire de Marie Unna = Hereditary hypotrichosis congenita: type Marie UnnaCHLEBAROV, S.H + G. Zeitschrift für Hautkrankheiten. 1985, Vol 60, Num 7, pp 583-596, issn 0301-0481, 8 p.Article

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