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Journal Abstract Search

162 related items for PubMed ID: 4141628

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  • 3. Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
    Ibsen HH, Clemmensen OJ, Brandrup F.
    Acta Derm Venereol; 1991; 71(4):349-51. PubMed ID: 1681656
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  • 4. Hereditary hypotrichosis. A previously undescribed syndrome.
    Bentley-Phillips B, Grace HJ.
    Br J Dermatol; 1979 Sep; 101(3):331-9. PubMed ID: 508598
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  • 6. Hereditary hypotrichosis simplex of the scalp.
    Rodríguez Díaz E, Fernández Blasco G, Martín Pascual A, Armijo M.
    Dermatology; 1995 Sep; 191(2):139-41. PubMed ID: 8520061
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  • 7. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B, Hundeiker M.
    Fortschr Med; 1979 Nov 22; 97(44):2018-22. PubMed ID: 511082
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  • 8. [Hypotrichosis congenita hereditaria Maria Unna].
    Wirth G, Bindewald I, Küster W, Goerz G.
    Hautarzt; 1985 Oct 22; 36(10):577-80. PubMed ID: 4066319
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  • 9. Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.
    Whyte MP, Petersen DJ, McAlister WH.
    Am J Med Genet; 1990 Jul 22; 36(3):288-91. PubMed ID: 2363424
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  • 10. Hereditary hypotrichosis simplex of the scalp.
    Vázquez MR, Rodríguez RR, Tapia AG, Diez LI.
    Pediatr Dermatol; 2002 Jul 22; 19(2):148-50. PubMed ID: 11994181
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  • 11. Hereditary hypotrichosis and localized morphea: a new clinical entity.
    Kulin P, Sybert VP.
    Pediatr Dermatol; 1986 Sep 22; 3(4):333-8. PubMed ID: 3774654
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  • 12. Congenital hypotrichosis due to short anagen.
    Barraud-Klenovsek MM, Trüeb RM.
    Br J Dermatol; 2000 Sep 22; 143(3):612-7. PubMed ID: 10971339
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  • 14. [Clinical investigation of a Chinese family with hypotrichosis simplex of the scalp and mutational analysis of CDSN gene].
    Huang XS, Jiang HO, Quan QL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug 22; 29(4):452-4. PubMed ID: 22875505
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  • 16. A sporadic case of congenital hypotrichosis simplex of the scalp: difficulties in diagnosis and classification.
    Cambiaghi S, Barbareschi M.
    Pediatr Dermatol; 1999 Aug 22; 16(4):301-4. PubMed ID: 10469417
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  • 17. Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
    Green J, Fitzpatrick E, de Berker D, Forrest SM, Sinclair RD.
    J Investig Dermatol Symp Proc; 2003 Jun 22; 8(1):121-5. PubMed ID: 12895008
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  • 18. Hereditary hypotrichosis (Marie Unna type).
    Peachey RD, Wells RS.
    Trans St Johns Hosp Dermatol Soc; 1971 Jun 22; 57(1):157-66. PubMed ID: 5570254
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  • 20. Hypotrichosis simplex of the scalp.
    Kanitakis J.
    J Eur Acad Dermatol Venereol; 2007 Nov 22; 21(10):1450. PubMed ID: 17958879
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