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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]
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]