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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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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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Does offering and performing prenatal screening influence women's attachment to their unborn child? A longitudinal randomized controlled trial

Prenatal diagnosis, 2007-08, Vol.27 (8), p.757-764

2007

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Unreported manifestations in two Dutch families with Bartsocas-Papas syndrome

American journal of medical genetics, 2003-12, Vol.123A (3), p.243-248

2003

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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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Human Uteroglobin Gene Polymorphisms and Genetic Susceptibility to Asthma

Annals of the New York Academy of Sciences, 2000-01, Vol.923 (1), p.303-306

2000

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Reply to Professor Niermeijer and Dr. Los

American journal of medical genetics, 1997-12, Vol.73 (4), p.490-490

ten Kate, Leo P.

1997

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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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A new family with the Townes-Brocks syndrome

Clinical genetics, 1988-09, Vol.34 (3), p.195-200

1988

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Malignant hemangiopericytoma in three kindred members of one family

Cancer, 1988-02, Vol.61 (4), p.841-844

1988

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Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes

American journal of medical genetics, 1992-06, Vol.43 (3), p.606-608

Kate, Leo P Ten

1992

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Effect of screening for cystic fibrosis on the influence of genetic counseling

Clinical genetics, 1987-10, Vol.32 (4), p.271-275

1987

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Comparison of couples referred and not referred for genetic counseling in a genetic clinic after the birth of a child with a congenital anomaly: A study in a population in the northeastern Netherlands

American journal of medical genetics, 1992-02, Vol.42 (3), p.387-392

1992

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Should parents be informed about the carrier status of their fetus?

American journal of medical genetics, 1996-10, Vol.65 (1), p.89-89

ten Kate, Leo P.

1996

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Prevalence of lethal osteochondrodysplasias

American journal of medical genetics, 1990-07, Vol.36 (3), p.377-378

1990

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Family distances can reveal hidden consanguinity

Clinical genetics, 1983-07, Vol.24 (1), p.29-35

1983

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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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Decreased scattering coefficient of blue sclerae

Clinical genetics, 1985-02, Vol.27 (2), p.187-190

1985

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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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The significance of different types of information in calculating the probability that a female relative of a Duchenne muscular dystrophy patient is a carrier

Clinical genetics, 1981-10, Vol.20 (4), p.281-288

1981

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Poland anomaly in mother and daughter

American journal of medical genetics, 1989-08, Vol.33 (4), p.519-521

1989

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Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]

American journal of medical genetics, 1993-09, Vol.47 (4), p.559-562

1993

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Association between ovulation stimulation, in vitro fertilisation, and neural tube defects?

Teratology (Philadelphia), 1990-09, Vol.42 (3), p.201-203

1990

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Duchenne muscular dystrophy inherited through paternal lines

American journal of medical genetics, 1992-01, Vol.42 (2), p.214-214

1992

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Risk of Down's syndrome among second- and third-degree relatives of a proband with trisomy 21

American journal of medical genetics, 1984-11, Vol.19 (3), p.599-600

1984

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

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

Does offering and performing prenatal screening influence women's attachment to their unborn child? A longitudinal randomized controlled trial

Unreported manifestations in two Dutch families with Bartsocas-Papas syndrome

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

Human Uteroglobin Gene Polymorphisms and Genetic Susceptibility to Asthma

Reply to Professor Niermeijer and Dr. Los

Community attitudes to cystic fibrosis carrier screening

A new family with the Townes-Brocks syndrome

Malignant hemangiopericytoma in three kindred members of one family

Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes

Effect of screening for cystic fibrosis on the influence of genetic counseling

Comparison of couples referred and not referred for genetic counseling in a genetic clinic after the birth of a child with a congenital anomaly: A study in a population in the northeastern Netherlands

Should parents be informed about the carrier status of their fetus?

Prevalence of lethal osteochondrodysplasias

Family distances can reveal hidden consanguinity

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

Decreased scattering coefficient of blue sclerae

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

The significance of different types of information in calculating the probability that a female relative of a Duchenne muscular dystrophy patient is a carrier

Poland anomaly in mother and daughter

Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]

Association between ovulation stimulation, in vitro fertilisation, and neural tube defects?

Duchenne muscular dystrophy inherited through paternal lines

Risk of Down's syndrome among second- and third-degree relatives of a proband with trisomy 21

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