BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 3774654)

  • 1. Hereditary hypotrichosis and localized morphea: a new clinical entity.
    Kulin P; Sybert VP
    Pediatr Dermatol; 1986 Sep; 3(4):333-8. PubMed ID: 3774654
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B; Hundeiker M
    Fortschr Med; 1979 Nov; 97(44):2018-22. PubMed ID: 511082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary hypotrichosis. A previously undescribed syndrome.
    Bentley-Phillips B; Grace HJ
    Br J Dermatol; 1979 Sep; 101(3):331-9. PubMed ID: 508598
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary hypotrichosis simplex of the scalp.
    Kohn G; Metzker A
    Clin Genet; 1987 Aug; 32(2):120-4. PubMed ID: 3652491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.
    Whyte MP; Petersen DJ; McAlister WH
    Am J Med Genet; 1990 Jul; 36(3):288-91. PubMed ID: 2363424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Hereditary hypotrichosis: a previously undescribed variant [proceedings].
    Bentley-Phillips B
    Br J Dermatol; 1978 Jul; 99(Suppl 16):12-3. PubMed ID: 698059
    [No Abstract]   [Full Text] [Related]  

  • 8. Two females with hair loss.
    Hermasch MA; Schön MP; Betz RC; Frank J
    J Dtsch Dermatol Ges; 2019 Aug; 17(8):845-847. PubMed ID: 31305016
    [No Abstract]   [Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary hypotrichosis (Marie-Unna type) (two cases).
    Hutchinson PE; Wells RS
    Proc R Soc Med; 1975 Aug; 68(8):534-5. PubMed ID: 1202498
    [No Abstract]   [Full Text] [Related]  

  • 11. Hereditary hypotrichosis of the scalp.
    Hess RO; Uno H
    Am J Med Genet; 1991 May; 39(2):125-9. PubMed ID: 2063912
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.
    He PP; Zhang XJ; Yang Q; Li M; Liang YH; Yang S; Yan KL; Cui Y; Shen YY; Wang HY; Sun LD; Du WH; Shen YJ; Xu SJ; Huang W
    Br J Dermatol; 2004 May; 150(5):837-42. PubMed ID: 15149494
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary hypotrichosis simplex of the scalp.
    Rodríguez Díaz E; Fernández Blasco G; Martín Pascual A; Armijo M
    Dermatology; 1995; 191(2):139-41. PubMed ID: 8520061
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N; Jordaan FH; Taljaard JJ; Hough SF
    Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].
    Mende B; Kreysel HW
    Hautarzt; 1987 Sep; 38(9):532-5. PubMed ID: 3692855
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Monilethrix: three cases.
    Penchaszadeh VB
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):262-4. PubMed ID: 5173278
    [No Abstract]   [Full Text] [Related]  

  • 17. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
    Wali A; Chishti M; Ayub M; Yasinzai M; Kafaitullah ; Ali G; John P; Ahmad W
    Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.
    Suga H; Tsunemi Y; Sugaya M; Shinkuma S; Akiyama M; Shimizu H; Sato S
    Acta Derm Venereol; 2011 Jun; 91(4):486-8. PubMed ID: 21537821
    [No Abstract]   [Full Text] [Related]  

  • 19. Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes.
    Cesarato N; Wehner M; Ghughunishvili M; Schmidt A; Axt D; Thiele H; Lentze MJ; Has C; Geyer M; Basmanav FB; Betz RC
    Am J Med Genet A; 2021 Dec; 185(12):3900-3904. PubMed ID: 34318586
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hereditary congenital hypotrichosis, Marie Unna type].
    Chlebarov S
    Z Hautkr; 1985 Apr; 60(7):583-96. PubMed ID: 4002769
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.