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6. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34. Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Eur J Hum Genet; 2001 Oct; 9(10):747-52. PubMed ID: 11781685 [Abstract] [Full Text] [Related]
7. [Van-der-Woude Syndrome]. Del Frari B, Amort M, Janecke AR, Schutte BC, Piza-Katzer H. Klin Padiatr; 2008 Oct; 220(1):26-8. PubMed ID: 18095255 [Abstract] [Full Text] [Related]
19. van der Woude syndrome in two families in China. Burdick AB, Ma LA, Dai ZH, Gao NN. J Craniofac Genet Dev Biol; 1987 Aug; 7(4):413-8. PubMed ID: 3429616 [Abstract] [Full Text] [Related]
20. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation. Beiraghi S, Miller-Chisholm A, Kimberling WJ, Sun CE, Wang YF, Russell LJ, Khoshnevisan M, Storm AL, Long RE, Witt PD, Mazaheri M, Diehl SR. J Craniofac Genet Dev Biol; 1999 Aug; 19(3):128-34. PubMed ID: 10589394 [Abstract] [Full Text] [Related] Page: [Next] [New Search]