Prenatal genetic diagnosis in 3000 amniocenteses.

Prenatal cytogenetic diagnosis of 1,400 consecutive amniocenteses.

Prenatal genetic diagnosis: current status.

Prenatal diagnosis of genetic disorders.

Prenatal diagnosis and genetic counseling.

Accuracy and safety of genetic prenatal diagnosis.

Ethical considerations of prenatal genetic diagnosis.

Invasive or non-invasive prenatal genetic diagnosis?

Editorial: Prenatal diagnosis and genetic counseling.

Genetic analysis of cystic fibrosis in Denmark. Implications for genetic counselling, carrier diagnosis and prenatal diagnosis.

Current concepts in genetics. Prenatal diagnosis of genetic disorders.

Molecular biological approaches to genetic disorders in prenatal diagnosis.

Challenges in prenatal and pre-implantation genetic diagnosis studies.

[Prenatal diagnosis of chromosome abnormalities and genetic metabolic disorders (proceedings)].

Prenatal diagnosis of hypophosphatasia; genetic, biochemical, and clinical studies.

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The "fetoscope"--a new clinical tool for prenatal genetic diagnosis.

Ethical and legal aspects of noninvasive prenatal genetic diagnosis.

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Prenatal cytogenetic diagnosis of 1,400 consecutive amniocenteses.

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Accuracy and safety of genetic prenatal diagnosis.

Ethical considerations of prenatal genetic diagnosis.

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Genetic analysis of cystic fibrosis in Denmark. Implications for genetic counselling, carrier diagnosis and prenatal diagnosis.

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Noninvasive prenatal testing: impact on genetic counseling, invasive prenatal diagnosis, and trisomy 21 detection.

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