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Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia.
Am J Hum Genet. 2013 Jan 10;92(1):88-98. doi: 10.1016/j.ajhg.2012.11.002. Epub 2012 Dec 20.
Am J Hum Genet. 2013.
PMID: 23261303
Free PMC article.
The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27.
Leegwater PA, Könst AA, Kuyt B, Sandkuijl LA, Naidu S, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS.
Leegwater PA, et al. Among authors: kuyt b.
Am J Hum Genet. 1999 Sep;65(3):728-34. doi: 10.1086/302548.
Am J Hum Genet. 1999.
PMID: 10441579
Free PMC article.
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Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36.
Zguricas J, Heus H, Morales-Peralta E, Breedveld G, Kuyt B, Mumcu EF, Bakker W, Akarsu N, Kay SP, Hovius SE, Heredero-Baute L, Oostra BA, Heutink P.
Zguricas J, et al. Among authors: kuyt b.
J Med Genet. 1999 Jan;36(1):32-40.
J Med Genet. 1999.
PMID: 9950363
Free PMC article.
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A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites.
de Vries Y, Lwiwski N, Levitus M, Kuyt B, Israels SJ, Arwert F, Zwaan M, Greenberg CR, Alter BP, Joenje H, Meijers-Heijboer H.
de Vries Y, et al. Among authors: kuyt b.
Anemia. 2012;2012:865170. doi: 10.1155/2012/865170. Epub 2012 Jun 4.
Anemia. 2012.
PMID: 22701786
Free PMC article.
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Incidence and survival of retinoblastoma in The Netherlands: a register based study 1862-1995.
Moll AC, Kuik DJ, Bouter LM, Den Otter W, Bezemer PD, Koten JW, Imhof SM, Kuyt BP, Tan KE.
Moll AC, et al. Among authors: kuyt bp.
Br J Ophthalmol. 1997 Jul;81(7):559-62. doi: 10.1136/bjo.81.7.559.
Br J Ophthalmol. 1997.
PMID: 9290369
Free PMC article.
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