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22. Genetic analysis in three Egyptian patients with Griscelli syndrome Type 1 reveals new nonsense mutations in MYO5A. Abd Elmaksoud MS; Gomaa NS; Azouz HG; On CNV; Ho CT; Omar TE; McGrath JA; Onoufriadis A Clin Exp Dermatol; 2020 Aug; 45(6):789-792. PubMed ID: 32275080 [No Abstract] [Full Text] [Related]
23. Waardenburg Syndrome type 1: A case report. Demirci GT; Atıs G; Altunay IK Dermatol Online J; 2011 Nov; 17(11):3. PubMed ID: 22136859 [TBL] [Abstract][Full Text] [Related]
24. Hearing impairment and pigmentary disturbance. Beighton P; Ramesar R; Winship I; Viljoen D; Greenberg J; Young K; Curtis D; Sellars S Ann N Y Acad Sci; 1991; 630():152-66. PubMed ID: 1952586 [TBL] [Abstract][Full Text] [Related]
26. Hypomelanotic conditions of the newborn and infant. Ruiz-Maldonado R Dermatol Clin; 2007 Jul; 25(3):373-82, ix. PubMed ID: 17662903 [TBL] [Abstract][Full Text] [Related]
27. Waardenburg syndrome type 2 in a Turkish family: implications for the importance of the pattern of fundus pigmentation. Müllner-Eidenböck A; Moser E; Frisch H; Read AP Br J Ophthalmol; 2001 Nov; 85(11):1384-6. PubMed ID: 11702731 [No Abstract] [Full Text] [Related]
28. [Leucoderma in children: Review of the literature]. Moulinas C; Dollfus H; Lipsker D Ann Dermatol Venereol; 2015; 142(6-7):399-409. PubMed ID: 25952794 [TBL] [Abstract][Full Text] [Related]
29. A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis. Grandin V; Sepulveda FE; Lambert N; Al Zahrani M; Al Idrissi E; Al-Mousa H; Almanjomi F; Al-Ghonaium A; K Habazi M; A Alghamdi H; Picard C; Bole-Feysot C; Nitschke P; Ménasché G; de Saint Basile G Hum Mutat; 2017 Oct; 38(10):1355-1359. PubMed ID: 28585352 [TBL] [Abstract][Full Text] [Related]
30. Albinism. Kinnear PE; Jay B; Witkop CJ Surv Ophthalmol; 1985; 30(2):75-101. PubMed ID: 3934778 [TBL] [Abstract][Full Text] [Related]
31. Striking contiguous depigmentation across the lower limbs in piebaldism and its implications for understanding melanocytic migration and development. Funkhouser CH; Kinsler VA; Frieden IJ Pediatr Dermatol; 2019 Jul; 36(4):511-513. PubMed ID: 30983016 [TBL] [Abstract][Full Text] [Related]
33. [Types of albinism and their ocular and cutaneous manifestations]. Käsmann-Kellner B Kinderkrankenschwester; 1999 Jun; 18(6):235-41. PubMed ID: 10514670 [No Abstract] [Full Text] [Related]
34. Pigmentary disorders in China. Zhang XJ; Yang S; Gao M Dermatol Clin; 2007 Jul; 25(3):439-47, x. PubMed ID: 17662909 [TBL] [Abstract][Full Text] [Related]
35. [Piebaldisme: a rare genodermatosis]. Debbarh FZ; Mernissi FZ Pan Afr Med J; 2017; 27():221. PubMed ID: 28979623 [TBL] [Abstract][Full Text] [Related]
36. Hereditary childhood hearing loss and integumentary system disease. Konigsmark BW J Pediatr; 1972 Jun; 80(6):909-19. PubMed ID: 5026034 [No Abstract] [Full Text] [Related]
37. Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion. Yılmaz M; Çağdaş D; Grandin V; Altıntaş DU; Tezcan İ; de Saint Basile G; Sanal Ö Pediatr Allergy Immunol; 2014 Dec; 25(8):817-9. PubMed ID: 25283056 [No Abstract] [Full Text] [Related]
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39. Genetic heterogeneity in Waardenburg's syndrome. Kulkarni ML; Kurian M; Guruprasad G; Panchakshariah MS J Med Genet; 1989 Jun; 26(6):411-2. PubMed ID: 2738907 [No Abstract] [Full Text] [Related]
40. Congenital poikiloderma with unusual hypopigmentation and acral blistering at birth. Ogunbiyi AO; Ogunbiyi JO; Baiyeroju-Agbeja AM J Eur Acad Dermatol Venereol; 1999 Jan; 12(1):54-8. PubMed ID: 10188152 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]