Article

Antenatal screening for genetic disease

1993-12-04

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: cb2c705d-8126-5ed4-ac3c-c72e39b969a7
DOI: 10.1136/bmj.307.6917.1498-b
PMCID: PMC1679491

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Antenatal screening for genetic diseaseDOI 10.1136/bmj.307.6917.1498-bRead

Prenatal genetic screening.Semantic proximity Read

Prenatal Genetic Testing OptionsSemantic proximity Read

Prenatal Diagnosis and ScreeningSemantic proximity Read

Carrier screening for recessive disordersSemantic proximity Read

Newborn Screening for Treatable Genetic Conditions: Past, Present and FutureSemantic proximity Read

Prenatal genetic carrier screening in the genomic ageSemantic proximity Read

Non-invasive prenatal diagnosis and screening for monogenic disordersSemantic proximity Read

Development of prenatal screening—A historical overviewSemantic proximity Read

Genetics in Obstetrics and GynecologySemantic proximity Read

Genetic diagnosis in the fetusSemantic proximity Read

Population programs for the detection of couples at risk for severe monogenic genetic diseasesSemantic proximity Read

8 Prenatal diagnosis and screening of the haemoglobinopathiesSemantic proximity Read