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Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study

BMC medical genetics, 2010-07, Vol.11 (1), p.113-113, Article 113

2010

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Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

Journal of cystic fibrosis, 2010-05, Vol.9 (3), p.165-178

2010

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First steps in exploring prospective exome sequencing of consanguineous couples

European journal of medical genetics, 2014-11, Vol.57 (11), p.613-616

2014

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Birth defects after incestuous mating: Calculating the probability of causality and reflecting on the desirability of genetic testing

European journal of medical genetics, 2013-05, Vol.56 (5), p.243-244

2013

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Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

BMC family practice, 2012-10, Vol.13, p.105

2012

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The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study

European journal of human genetics : EJHG, 2005-08, Vol.13 (8), p.947-952

2005

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Segregation ratio in cranio-cerebello-cardiac syndrome

European journal of human genetics : EJHG, 2006-09, Vol.14 (9), p.1054-1057

2006

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Polymorphisms in the tumor necrosis factor and lymphotoxin-α gene region and preeclampsia

Obstetrics and gynecology (New York. 1953), 2001, Vol.98 (4), p.612-619

2001

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Does Prenatal Screening Influence Anxiety Levels of Pregnant Women? A Longitudinal Randomized Controlled Trial

Obstetrical & gynecological survey, 2006-10, Vol.61 (10), p.632-633

2006

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Polymorphisms in the Tumor Necrosis Factor and Lymphotoxin-α Gene Region and Preeclampsia

Obstetrics and gynecology (New York. 1953), 2001-10, Vol.98 (4), p.612-619

2001

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Phase I safety assessment of intrathecal ketorolac

Pain (Amsterdam), 2002-10, Vol.99 (3), p.599-604

2002

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Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease

Kidney international, 1990-11, Vol.38 (5), p.880-885

1990

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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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Community attitudes to cystic fibrosis carrier screening

Prenatal diagnosis, 1990-04, Vol.10 (4), p.275-276

1990

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Carrier screening for Tay-Sachs disease and cystic fibrosis

The Lancet (British edition), 1990-06, Vol.335 (8704), p.1527-1528

1990

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A method for analysing fertility of heterozygotes for autosomal recessive disorders, with special reference to cystic fibrosis, Tay‐Sachs disease and phenylketonuria

Annals of human genetics, 1977-01, Vol.40 (3), p.287-297

KATE, LEO P. Ten

1977

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On estimating the actual rate of foetal loss in families with an autosomal recessive disorder and Woolf's data on PKU

Annals of human genetics, 1978-05, Vol.41 (4), p.463-464

KATE, LEO P. ten

1978

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Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study

Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

First steps in exploring prospective exome sequencing of consanguineous couples

Birth defects after incestuous mating: Calculating the probability of causality and reflecting on the desirability of genetic testing

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study

Segregation ratio in cranio-cerebello-cardiac syndrome

Polymorphisms in the tumor necrosis factor and lymphotoxin-α gene region and preeclampsia

Does Prenatal Screening Influence Anxiety Levels of Pregnant Women? A Longitudinal Randomized Controlled Trial

Polymorphisms in the Tumor Necrosis Factor and Lymphotoxin-α Gene Region and Preeclampsia

Phase I safety assessment of intrathecal ketorolac

Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease

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

Community attitudes to cystic fibrosis carrier screening

Carrier screening for Tay-Sachs disease and cystic fibrosis

A method for analysing fertility of heterozygotes for autosomal recessive disorders, with special reference to cystic fibrosis, Tay‐Sachs disease and phenylketonuria

On estimating the actual rate of foetal loss in families with an autosomal recessive disorder and Woolf's data on PKU

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