Family history and DNA analysis in patients with suspected Huntington's disease

Por Siesling, S, de Vlis, M V.-v., Losekoot, M, Belfroid, R, Maat-Kievit, J, Kremer, H, Roos, R
Publicado em 2000

Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities

Por d Helderman-van, Maaswinkel-Mooij, P, Hoogendoorn, E, Willemsen, R, Maat-Kievit, J, Losekoot, M, Oostra, B
Publicado em 1999

A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15

Por Breedveld, G, van Wetten, B, te Raa, G D, Brusse, E, van Swieten, J C, Oostra, B, Maat-Kievit, J
Publicado em 2004

Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations

Por Elfferich, Peter, Verleun-Mooijman, Marja C., Maat-Kievit, J. Anneke, van de Warrenburg, Bart P. C., Abdo, Wilson F., Eshuis, Sylvia A., Leenders, Klaus L., Hovestadt, Ad, Zijlmans, Jan C. M., Stroy, Jan-Pieter M., van Swieten, John C., Boon, Agnita J. W., van Engelen, Klaartje, Verschuuren-Bemelmans, Corien C., Lesnik-Oberstein, Saskia A. J., Tassorelli, Cristina, Lopiano, Leonardo, Bonifati, Vincenzo, Dooijes, Dennis, van Minkelen, Rick
Publicado em 2011