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Relative frequencies of cystic fibrosis mutations in The netherlands as an illustration of significant regional variation in a small country

Human genetics, 1998-05, Vol.102 (5), p.587-590

1998

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Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations

Human genetics, 1996-09, Vol.98 (3), p.304-309

1996

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Validation of the determination of ΔF508 mutations of the cystic fibrosis gene in over 11000 mouthwashes

Human genetics, 1996, Vol.97 (3), p.334-336

1996

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Prevalence of carriers of the most common medium-chain acyl-CoA dehydrogenase (MCAD) deficiency mutation (G985A) in the Netherlands

Human genetics, 1996-07, Vol.98 (1), p.1-2

1996

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Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene : a European study

Human genetics, 1992, Vol.88 (3), p.249-257

1992

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Birth and population prevalence of Duchenne muscular dystrophy in the Netherlands

Human genetics, 1992, Vol.88 (3), p.258-266

1992

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Down syndrome : effects of demographic factors and prenatal diagnosis on the future livebirth prevalence

Human genetics, 1993-09, Vol.92 (2), p.163-168

1993

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Consanguinity sans reproche

Human genetics, 1991, Vol.86 (3), p.295-296

1991

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Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibrium

Human genetics, 1990-09, Vol.85 (4), p.425-427

1990

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Ascertainment bias and power of procedures to estimate differences between male and female mutation rates

Human genetics, 1987-03, Vol.75 (3), p.296-296

1987

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Relative frequencies of cystic fibrosis mutations in The netherlands as an illustration of significant regional variation in a small country

Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations

Validation of the determination of ΔF508 mutations of the cystic fibrosis gene in over 11000 mouthwashes

Prevalence of carriers of the most common medium-chain acyl-CoA dehydrogenase (MCAD) deficiency mutation (G985A) in the Netherlands

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene : a European study

Birth and population prevalence of Duchenne muscular dystrophy in the Netherlands

Down syndrome : effects of demographic factors and prenatal diagnosis on the future livebirth prevalence

Consanguinity sans reproche

Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibrium

Ascertainment bias and power of procedures to estimate differences between male and female mutation rates

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