These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 4847756)

  • 1. Hereditary hyperpigmentation anomalies in blacks.
    Pierce ER; Teneyck FD
    J Hered; 1974; 65(3):157-9. PubMed ID: 4847756
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial progressive hyperpigmentation.
    Chernosky ME; Anderson DE; Chang JP; Shaw MW; Romsdahl MM
    Arch Dermatol; 1971 Jun; 103(6):581-91 passim. PubMed ID: 4326548
    [No Abstract]   [Full Text] [Related]  

  • 3. Hereditary diffuse hyperpigmentation.
    Verbov J
    Clin Exp Dermatol; 1980 Jun; 5(2):227-34. PubMed ID: 7438517
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary congenital severe deafness syndromes.
    Konigsmark BW
    Ann Otol Rhinol Laryngol; 1971 Apr; 80(2):269-88. PubMed ID: 4927796
    [No Abstract]   [Full Text] [Related]  

  • 5. [Piebaldism].
    Küster W
    Hautarzt; 1987 Aug; 38(8):481-3. PubMed ID: 3654219
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary sclerosing poikiloderma. Report of two families with an unusual and distinctive genodermatosis.
    Weary PE; Hsu YT; Richardson DR; Caravati CM; Wood BT
    Arch Dermatol; 1969 Oct; 100(4):413-22. PubMed ID: 5358102
    [No Abstract]   [Full Text] [Related]  

  • 7. Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria.
    Lu C; Liu J; Liu F; Liu Y; Ma D; Zhang X
    J Dermatol Sci; 2014 Dec; 76(3):255-8. PubMed ID: 25288164
    [No Abstract]   [Full Text] [Related]  

  • 8. Hyperpigmentation of pernicious anemia in blacks. Report of three cases.
    Ogbuawa O; Trowell J; Williams JT; Bradley C; Archer J; Henry L
    Arch Intern Med; 1978 Mar; 138(3):388-9. PubMed ID: 629633
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Generalized mottled pigmentation with postnatal skin blistering in three generations.
    Westerhof W; Dingemans KP
    J Am Acad Dermatol; 2004 May; 50(5 Suppl):S65-9. PubMed ID: 15097931
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CFC syndrome: report of familial cases.
    Lecora M; Parenti G; Andria G
    Clin Genet; 1996 Dec; 50(6):558-9. PubMed ID: 9147900
    [No Abstract]   [Full Text] [Related]  

  • 11. Periorbital hyperpigmentation. An overlooked genetic disorder of pigmentation.
    Goodman RM; Belcher RW
    Arch Dermatol; 1969 Aug; 100(2):169-74. PubMed ID: 5797956
    [No Abstract]   [Full Text] [Related]  

  • 12. Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in south-east Germany.
    Zanardo L; Stolz W; Schmitz G; Kaminski W; Vikkula M; Landthaler M; Vogt T
    Acta Derm Venereol; 2004; 84(1):57-60. PubMed ID: 15040480
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Selection against lethal alleles in females heterozygous for incontinentia pigmenti.
    Migeon BR; Axelman J; Jan de Beur S; Valle D; Mitchell GA; Rosenbaum KN
    Am J Hum Genet; 1989 Jan; 44(1):100-6. PubMed ID: 2562819
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Epidermolysis bullosa simplex and mottled pigmentation: a new dominant syndrome. I. Clinical and histological features.
    Fischer T; Gedde-Dahl T
    Clin Genet; 1979 Mar; 15(3):228-38. PubMed ID: 421361
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hyperpigmentation and hypohidrosis. (The Naegeli-Franceschetti-Jadassohn syndrome): report of a family and review of the literature.
    Sparrow GP; Samman PD; Wells RS
    Clin Exp Dermatol; 1976 Jun; 1(2):127-40. PubMed ID: 939040
    [No Abstract]   [Full Text] [Related]  

  • 16. [Incontinentia pigmenti. Study of 3 families].
    Garcia-Bravo B; Rodriguez-Pichardo A; Camacho-Martinez F
    Ann Dermatol Venereol; 1986; 113(4):301-8. PubMed ID: 3767228
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A "new" autosomal dominant genodermatosis characterized by hyperpigmented spots and plamoplantar hyperkeratosis.
    Cantú JM; Sánchez-Corona J; Fragoso R; Macotela-Ruiz E; Garciá-Cruz D
    Clin Genet; 1978 Sep; 14(3):165-8. PubMed ID: 151611
    [TBL] [Abstract][Full Text] [Related]  

  • 18. On the inheritance of incontinentia pigmenti.
    Cantu-Garza JM; Ruiz-Barquin E
    Dermatologica; 1971; 143(3):190-7. PubMed ID: 5316159
    [No Abstract]   [Full Text] [Related]  

  • 19. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P; Zerres K
    Am J Med Genet; 1993 Mar; 45(5):642-8. PubMed ID: 8456838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
    Amini-Elihou S
    J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.