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5. Familial multiforme ventricular extrasystoles with short stature, hyperpigmentation and microcephaly-a new syndrome. Char F; Douglas JE; Dungan WT Birth Defects Orig Artic Ser; 1975; 11(5):63-9. PubMed ID: 1218236 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering: a clinical triad, with variable associations. A report of two families. Boss JM; Matthews CN; Peachey RD; Summerly R Br J Dermatol; 1981 Nov; 105(5):579-85. PubMed ID: 6457621 [No Abstract] [Full Text] [Related]
9. [Pathology and genetics of bipalperbral hyperpigmentation]. Aguilera Díaz L Actas Dermosifiliogr; 1971; 62(9):397-410. PubMed ID: 5155116 [No Abstract] [Full Text] [Related]
10. Familial progressive hyperpigmentation: a family study in China. Ling DB; Lo T Br J Dermatol; 1991 Dec; 125(6):607. PubMed ID: 1760373 [No Abstract] [Full Text] [Related]
11. Incontinentia pigmenti: a chromosomal breakage syndrome. Kelly TE; Rary JM; Young L J Hered; 1976; 67(3):171-2. PubMed ID: 939916 [No Abstract] [Full Text] [Related]
12. 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]
14. Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome. Abdallat A; Davis SM; Farrage J; McDonald WI J Neurol Neurosurg Psychiatry; 1980 Nov; 43(11):962-6. PubMed ID: 7441281 [TBL] [Abstract][Full Text] [Related]
15. X-linked short stature with skin pigmentation: evidence for heterogeneity of the Russell-Silver syndrome. Partington MW Clin Genet; 1986 Feb; 29(2):151-6. PubMed ID: 3955866 [TBL] [Abstract][Full Text] [Related]
16. An Arab family with Waardenburg syndrome. Amin-Zaki L J Laryngol Otol; 1971 May; 85(5):471-80. PubMed ID: 5580051 [No Abstract] [Full Text] [Related]