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	1.	Trisomy 1q42 --> qter in a sister and brother: further delineation of the "trisomy 1q42 --> qter syndrome". [electronic resource] by Verschuuren-Bemelmans, C C Leegte, B Hodenius, T M Cobben, J M Producer: 19951120 In: American journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Trisomy 12 mosaicism in CVS culture confirmed in the fetus. [electronic resource] by Sikkema-Raddatz, B Bouman, K Verschuuren-Bemelmans, C C de Jong, B Producer: 20000330 In: Prenatal diagnosis vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	3.	A 46,XX,der(13;14)(q10;q10),+21 child born after a 45,XX,der(13;14)(q10;q10) chromosomal finding in CVS. [electronic resource] by Sikkema-Raddatz, B Verschuuren-Bemelmans, C C Kloosterman, M de Jong, B Producer: 19980129 In: Prenatal diagnosis vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Four years' cytogenetic experience with the culture of chorionic villi. [electronic resource] by Sikkema-Raddatz, B Bouman, K Verschuuren-Bemelmans, C C Stoepker, M Mantingh, A Beekhuis, J R de Jong, B Producer: 20010109 In: Prenatal diagnosis vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	5.	Trends in live birth prevalence of down syndrome in the Northern Netherlands 1987-96: the impact of screening and prenatal diagnosis. [electronic resource] by Wortelboer, M J De Wolf, B T Verschuuren-Bemelmans, C C Reefhuis, J Mantingh, A Beekhuis, J R Cornel, M C Producer: 20001025 In: Prenatal diagnosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Striatal dopamine D2 receptors, metabolism, and volume in preclinical Huntington disease. [electronic resource] by van Oostrom, J C H Maguire, R P Verschuuren-Bemelmans, C C Veenma-van der Duin, L Pruim, J Roos, R A C Leenders, K L Producer: 20060310 In: Neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Thrombocytopenia-absent radius syndrome: a clinical genetic study. [electronic resource] by Greenhalgh, K L Howell, R T Bottani, A Ancliff, P J Brunner, H G Verschuuren-Bemelmans, C C Vernon, E Brown, K W Newbury-Ecob, R A Producer: 20030312 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect. [electronic resource] by Rump, P Lemmink, H H Verschuuren-Bemelmans, C C Grootscholten, P M Fock, J M Hayflick, S J Westaway, S K Vos, Y J van Essen, A J Producer: 20060814 In: Neurogenetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I. [electronic resource] by Verschuuren-Bemelmans, C C Brunt, E R Burton, M Mensink, R G van der Meulen, M A Smit, N H Stolte-Dijkstra, I Buys, C H Scheffer, H Producer: 19960122 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Neurophysiological evaluation in children with Friedreich's ataxia. [electronic resource] by Sival, D A du Marchie Sarvaas, G J Brouwer, O F Uges, D R Verschuuren-Bemelmans, C C Maurits, N M Brunt, E R van der Hoeven, J H Producer: 20100212 In: Early human development vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers. [electronic resource] by van Gaalen, J Maas, R P P W M Ippel, E F Elting, M W van Spaendonck-Zwarts, K Y Vermeer, S Verschuuren-Bemelmans, C Timmann, D van de Warrenburg, Bart P Producer: 20190603 In: Experimental brain research vol. 237 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Counselling following the Prenatal Diagnosis of Klinefelter Syndrome: Comparisons between Geneticists and Obstetricians in Five European Countries. [electronic resource] by Hall, S Marteau, T.M Limbert, C Reid, M Feijóo, M Soares, M Nippert, I Bobrow, M Cameron, A Van Diem, M Verschuuren-Bemelmans, C Eiben, B García-Miñaur, S Walkinshaw, S Soothill, P De Vigan, C McIntosh, K Kirwan, D Publication details: Community genetics Jun 2001 In: Community genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis. [electronic resource] by van de Warrenburg, B P C Sinke, R J Verschuuren-Bemelmans, C C Scheffer, H Brunt, E R Ippel, P F Maat-Kievit, J A Dooijes, D Notermans, N C Lindhout, D Knoers, N V A M Kremer, H P H Producer: 20020419 In: Neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	RYR1-related myopathies: a wide spectrum of phenotypes throughout life. [electronic resource] by Snoeck, M van Engelen, B G M Küsters, B Lammens, M Meijer, R Molenaar, J P F Raaphorst, J Verschuuren-Bemelmans, C C Straathof, C S M Sie, L T L de Coo, I F van der Pol, W L de Visser, M Scheffer, H Treves, S Jungbluth, H Voermans, N C Kamsteeg, E-J Producer: 20160129 In: European journal of neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008. [electronic resource] by van Rij, M C de Koning Gans, P A M Aalfs, C M Elting, M Ippel, P F Maat-Kievit, J A Vermeer, S Verschuuren-Bemelmans, C C van Belzen, M J Belfroid, R D M Losekoot, M Geraedts, J P M Roos, R A C Tibben, A de Die-Smulders, C E M Bijlsma, E K Producer: 20140718 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A clinical diagnostic algorithm for early onset cerebellar ataxia. [electronic resource] by Brandsma, R Verschuuren-Bemelmans, C C Amrom, D Barisic, N Baxter, P Bertini, E Blumkin, L Brankovic-Sreckovic, V Brouwer, O F Bürk, K Catsman-Berrevoets, C E Craiu, D de Coo, I F M Gburek, J Kennedy, C de Koning, T J Kremer, H P H Kumar, R Macaya, A Micalizzi, A Mirabelli-Badenier, M Nemeth, A Nuovo, S Poll-The, B Lerman-Sagie, T Steinlin, M Synofzik, M Tijssen, M A J Vasco, G Willemsen, M A A P Zanni, G Valente, E M Boltshauser, E Sival, D A Producer: 20200113 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)