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1. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range. Issue 12 (December 1993)

7. Neonatal onset autosomal dominant polycystic kidney disease (ADPKD) in a patient homozygous for a PKD2 missense mutation due to uniparental disomy. Issue 1 (23rd November 2011)

9. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. Issue 11 (November 1997)

10. Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008. (27th March 2013)