1Scherer SW,Poorkaj P,MaSSa H,et al.Physical mapping of the split hand/split foot locus on chromoSome 7 and implication in syndromic ectrodactyly.Hum Molec Genet 1994;3:1345-1354.
2Zheng J,Shen W.Prestin is the motor protein of cochlear outer hair cells.Nature 2000;405:149-155.
3van Steensel M,Smith FJD,Steijlen PM,et al.The gene for hypertrichosis of Marie Unna maps between D8S258 and D8S298:exclusion of the hr gene by cDNA and genomic Sequencing.Am J Hum Genet 1999;65:413-419.
4Sreekumar GP,Roberts JL,Wong CQ,et al.Marie unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless.J Invest Dermatol 2000; 114:595-597.
5Lefevre P,Rochat A,Bodemer C,et al.Linkage of marie-unna hypotrichosis locus to chromosome 8p21 and excluSion of 10 genes including the hairless gene by mutation analysis.Europ J Hum Genet 2000;8:273-279.
6Ignata C,Fiore M,Guzzetta V,et al.Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs.Am J Med Genet 1996;65:167-170.
7Adriani M,Martinez-Mir A,Fusco F,et al.Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.Ann Hum Genet 2004; 68:265-268.
8Baumer A,Belli S,Trueb RM,et al.An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an italian family.Europ J Hum Genet 2000; 8:443-448.
9Miller J,Djabali K,Chen T,et al.Atrichia caused by mutationS in the vitamin D receptorgene is a phenocopy of generalized atrichia caused by mutations in the hairless gene.J Invest Dermatol 2001;117:612-617.
10Ahmad W,Haque MF,Brancolini V,et al.Alopecia universalis associated with a mutation in the human hairless gene.Science 1998; 279:720-724.