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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

Volltextzugriff (PDF)

Carrier screening in CF

Nature (London), 1989-11, Vol.342 (6246), p.131-131

TEN KATE, LEO P

1989

Volltextzugriff (PDF)

Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome

American journal of human genetics, 1999-02, Vol.64 (2), p.435-445

1999

Volltextzugriff (PDF)

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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Survival and clinical outcome in patients with cystic fibrosis, with or without neonatal screening

The Journal of pediatrics, 1989-03, Vol.114 (3), p.362-367

1989

Volltextzugriff (PDF)

Familial aggregation of coronary heart disease and its relation to known genetic risk factors

The American journal of cardiology, 1982-11, Vol.50 (5), p.945-953

1982

Volltextzugriff (PDF)

OVULATION INDUCTION AND NEURAL TUBE DEFECTS

The Lancet (British edition), 1989-06, Vol.333 (8651), p.1386-1386

1989

Volltextzugriff (PDF)

Carrier screening for Tay-Sachs disease and cystic fibrosis

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

1990

Volltextzugriff (PDF)

OVULATION INDUCTION, IN-VITRO FERTILISATION, AND NEURAL TUBE DEFECTS

The Lancet (British edition), 1989-12, Vol.334 (8678), p.1530-1530

1989

Volltextzugriff (PDF)

Malignant hemangiopericytoma in three kindred members of one family

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

1988

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PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

The Lancet (British edition), 1988-12, Vol.332 (8623), p.1319-1319

1988

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PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WHERE SINGLE AFFECTED CHILD HAS DIED

The Lancet (British edition), 1988-09, Vol.332 (8613), p.745-745

1988

Volltextzugriff (PDF)

Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: Assortative mating for lifestyle and risk factors?

The American journal of cardiology, 1984-02, Vol.53 (4), p.399-403

1984

Volltextzugriff (PDF)

RAPID SCREENING FOR ΔF508 DELETION IN CYSTIC FIBROSIS

The Lancet (British edition), 1989-12, Vol.334 (8675), p.1345-1346

1989

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

Carrier screening in CF

Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome

Human Uteroglobin Gene Polymorphisms and Genetic Susceptibility to Asthma

Survival and clinical outcome in patients with cystic fibrosis, with or without neonatal screening

Familial aggregation of coronary heart disease and its relation to known genetic risk factors

OVULATION INDUCTION AND NEURAL TUBE DEFECTS

Carrier screening for Tay-Sachs disease and cystic fibrosis

OVULATION INDUCTION, IN-VITRO FERTILISATION, AND NEURAL TUBE DEFECTS

Malignant hemangiopericytoma in three kindred members of one family

PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WHERE SINGLE AFFECTED CHILD HAS DIED

Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: Assortative mating for lifestyle and risk factors?

RAPID SCREENING FOR ΔF508 DELETION IN CYSTIC FIBROSIS

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