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

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

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

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

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

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 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

Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations : A new autosomal dominant syndromeWHYTE, M. P; PETERSEN, D. J; MCALISTER, W. H et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 288-291, issn 0148-7299, 4 p.Article

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani familiesWASIF, Naveed; UL-HASSAN NAQVI, Syed Kamran; NADIR ALI, Sulman Basit et al.Human genetics. 2011, Vol 129, Num 4, pp 419-424, issn 0340-6717, 6 p.Article

Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3-p22.3 in a Pakistani family and screening of the candidate genesBASIT, Sulman; ALI, Ghazanfar; WASIF, Naveed et al.Human genetics. 2010, Vol 128, Num 2, pp 213-220, issn 0340-6717, 8 p.Article

Implication du récepteur P2Y5 et de son ligand LPA dans l'hypotrichose simplex et le syndrome des cheveux laineux autosomique récessif = Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndromeDEREURE, O.Annales de dermatologie et de vénéréologie. 2008, Vol 135, Num 11, pp 794-795, issn 0151-9638, 2 p.Article

Total hypotrichosis : genetic form of alopecia not linked to hairless geneROGAEV, E. I; ZINCHENKO, R. A; DVORYACHIKOV, G et al.Lancet (British edition). 1999, Vol 354, Num 9184, pp 1097-1098, issn 0140-6736Article

Identification of LIFH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotypeSAYED HAJAN SHAH; ABID, Aiysha; SHAHID, Saba et al.Journal of the Pakistan Medical Association. 2011, Vol 61, Num 11, pp 1060-1064, issn 0030-9982, 5 p.Article

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplexSHIMOMURA, Yutaka; AGALLIU, Dritan; BARRES, Ben A et al.Nature (London). 2010, Vol 464, Num 7291, pp 1043-1047, issn 0028-0836, 5 p.Article

Ichtyose récessive autosornique avec hypotrichose et mutation de ST 14 = Receive autosomal ichthyosis with hypotrichosis with mutationDEREURE, O.Annales de dermatologie et de vénéréologie. 2007, Vol 134, Num 10, pp 798-798, issn 0151-9638, 1 p., CAH1Article