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22. Clinical and scanning electron microscopic findings in a solitary case of Trichorhinophalangeal syndrome type I. Prens EP; Peereboom-Wynia JD; de Bruyn WC; van Joost T; Stolz E Acta Derm Venereol; 1984; 64(3):249-53. PubMed ID: 6204489 [TBL] [Abstract][Full Text] [Related]
23. [Study of hair in type I tricho-rhino-phalangeal syndrome]. Lalević-Vasić BM; Nikolić MM; Polić DJ Ann Dermatol Venereol; 1994; 121(9):618-22. PubMed ID: 7771728 [TBL] [Abstract][Full Text] [Related]
24. Marie Unna hypotrichosis in a Chinese family. Wong SN; Giam YC; Lee YS Pediatr Dermatol; 2002; 19(3):250-5. PubMed ID: 12047647 [TBL] [Abstract][Full Text] [Related]
25. Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report. Redler S; Kruse R; Eigelshoven S; Hanneken S; Refke M; Wen Y; Zhang X; Cichon S; Betz RC; Nöthen MM J Am Acad Dermatol; 2011 Apr; 64(4):e45-50. PubMed ID: 20659777 [TBL] [Abstract][Full Text] [Related]
26. An unusual defect resembling pili bifurcati. Sala F; Crosti C; Bencini PL; Menni S Arch Dermatol; 1985 Jun; 121(6):718. PubMed ID: 4004299 [No Abstract] [Full Text] [Related]
27. Hypotrichosis and nail dysplasia: a novel hidrotic ectodermal dysplasia. Harrison S; Sinclair R Australas J Dermatol; 2004 May; 45(2):103-5. PubMed ID: 15068456 [TBL] [Abstract][Full Text] [Related]
28. Marie Unna congenital hypotrichosis: clinical description, histopathology, scanning electron microscopy of a previously unreported large pedigree. Roberts JL; Whiting DA; Henry D; Basler G; Woolf L J Investig Dermatol Symp Proc; 1999 Dec; 4(3):261-7. PubMed ID: 10674378 [TBL] [Abstract][Full Text] [Related]
30. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis. Lefevre P; Rochat A; Bodemer C; Vabres P; Barrandon Y; de Prost Y; Garner C; Hovnanian A Eur J Hum Genet; 2000 Apr; 8(4):273-9. PubMed ID: 10854110 [TBL] [Abstract][Full Text] [Related]
31. Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance. Toribio J; Quiñones PA Br J Dermatol; 1974 Dec; 91(6):687-96. PubMed ID: 4141628 [No Abstract] [Full Text] [Related]
32. Marie Unna hypotrichosis in an Asian family. Kim HS; Kim SC; Lee WS J Dermatol; 2001 Mar; 28(3):149-52. PubMed ID: 11349466 [TBL] [Abstract][Full Text] [Related]
33. Hypotrichosis with keratosis pilaris: electrophoretical study of hair fibrous proteins from a patient. Dekio S; Nagashima T; Watanabe Y; Jidoi J Dermatologica; 1989; 179(3):118-22. PubMed ID: 2591617 [TBL] [Abstract][Full Text] [Related]
34. [A syndrome: uncombable hair. Observation of 6 members of a family with pili canaliculi, associated with pili torti, progressive alopecia, atopic eczema and hamartomas]. Braun-Falco O; Ryckmanns F; Heilgemeir GP; Ring J Hautarzt; 1982 Jul; 33(7):366-72. PubMed ID: 7107281 [TBL] [Abstract][Full Text] [Related]
35. Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair. Horev L; Tosti A; Rosen I; Hershko K; Vincenzi C; Nanova K; Mali A; Potikha T; Zlotogorski A J Am Acad Dermatol; 2009 Nov; 61(5):813-8. PubMed ID: 19766349 [TBL] [Abstract][Full Text] [Related]
36. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities. Farkas K; Nagy N; Kinyó A; Kemény L; Széll M Arch Dermatol Res; 2012 Oct; 304(8):679-81. PubMed ID: 22584530 [TBL] [Abstract][Full Text] [Related]
37. Hypotrichosis, hair structure defects, hypercysteine hair and glucosuria: a new genetic syndrome? Blume-Peytavi U; Föhles J; Schulz R; Wortmann G; Gollnick H; Orfanos CE Br J Dermatol; 1996 Feb; 134(2):319-24. PubMed ID: 8746349 [TBL] [Abstract][Full Text] [Related]
38. Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity. Yan KL; He PP; Yang S; Li M; Yang Q; Ren YQ; Cui Y; Gao M; Xiao FL; Huang W; Zhang XJ Clin Exp Dermatol; 2004 Sep; 29(5):460-3. PubMed ID: 15347323 [TBL] [Abstract][Full Text] [Related]
39. [Erythrodermia ichthyosiformis congenita with hypotrichosis, anhidrosis, deaf-mutism and decreased elimination of various amino acids in the urine]. Salamon T; Budai V; Lazović O; Macanović K; Volić N Hautarzt; 1974 Sep; 25(9):448-53. PubMed ID: 4617749 [No Abstract] [Full Text] [Related]
40. Marie-Unna hereditary hypotrichosis: case report and review of the literature. Podjasek JO; Hand JL Pediatr Dermatol; 2011; 28(2):202-4. PubMed ID: 21504454 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]