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Preconception Care for Consanguineous Couples in the Netherlands

Cousin Marriages, 2015, Vol.28, p.202

1, 2015

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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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Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism

European journal of human genetics : EJHG, 2012-07, Vol.20 (7), p.729-733

2012

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Does informed decision making influence psychological outcomes after receiving a positive screening outcome?

Prenatal diagnosis, 2009-03, Vol.29 (3), p.271-273

2009

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Informed decision making in the context of prenatal screening

Patient education and counseling, 2006-10, Vol.63 (1), p.110-117

2006

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Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial

Prenatal diagnosis, 2006-04, Vol.26 (4), p.354-361

2006

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Are pregnant women making informed choices about prenatal screening?

Genetics in medicine, 2005-05, Vol.7 (5), p.332-338

2005

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The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas

Molecular human reproduction, 2004-08, Vol.10 (8), p.589-598

2004

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Attitudes of Potential Providers Towards Preconceptional Cystic Fibrosis Carrier Screening

Journal of genetic counseling, 2004-02, Vol.13 (1), p.31-44

2004

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Searching for preeclampsia genes: the current position

European journal of obstetrics & gynecology and reproductive biology, 2002-11, Vol.105 (2), p.94-113

2002

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Personal experiences of cystic fibrosis (CF) carrier couples prospectively identified in CF families

American journal of medical genetics, 2002-07, Vol.110 (4), p.324-331

2002

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Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

Genetics in medicine, 2002-07, Vol.4 (4), p.241-249

2002

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LINKAGE AND ASSOCIATION STUDIES OF IL1B AND IL1RN GENE POLYMORPHISMS IN PREECLAMPSIA

Hypertension in pregnancy, 2002, Vol.21 (1), p.23-38

2002

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A genome-wide scan for preeclampsia in the Netherlands

European journal of human genetics : EJHG, 2001-10, Vol.9 (10), p.758-764

2001

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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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Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia

American journal of obstetrics and gynecology, 2001-02, Vol.184 (3), p.394-402

2001

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Screening for cystic fibrosis and its evaluation

British medical bulletin, 1998, Vol.54 (4), p.857-875

1998

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The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol

Journal of medical genetics, 1997-10, Vol.34 (10), p.805-812

1997

Volltextzugriff (PDF)

Identification of the cystic fibrosis gene

BMJ (Online), 1990-04, Vol.300 (6730), p.1015

1990

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Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982

Journal of epidemiology and community health (1979), 1988-09, Vol.42 (3), p.266-270

1988

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Serum creatine-kinase (CK) in normal pregnancy

American journal of medical genetics, 1983-08, Vol.15 (4), p.665-667

1983

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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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Preconception Care for Consanguineous Couples in the Netherlands

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

Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism

Does informed decision making influence psychological outcomes after receiving a positive screening outcome?

Informed decision making in the context of prenatal screening

Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial

Are pregnant women making informed choices about prenatal screening?

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas

Attitudes of Potential Providers Towards Preconceptional Cystic Fibrosis Carrier Screening

Searching for preeclampsia genes: the current position

Personal experiences of cystic fibrosis (CF) carrier couples prospectively identified in CF families

Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

LINKAGE AND ASSOCIATION STUDIES OF IL1B AND IL1RN GENE POLYMORPHISMS IN PREECLAMPSIA

A genome-wide scan for preeclampsia in the Netherlands

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

Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia

Screening for cystic fibrosis and its evaluation

The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol

Identification of the cystic fibrosis gene

Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982

Serum creatine-kinase (CK) in normal pregnancy

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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