Prenatal diagnosis of common genetic disorders.

Author:

Crawfurd M. D.

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference64 articles.

1. IPrenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficicncv by steroid analysis in the amniotic fluid of midpregnancy; comparison with HLA typing in 17 pregnancies at risk for CAH;Forest, M.G.; Betuel, H.; Couillin, P.; Boue, A.,1981

2. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiencyv by HLA typing;Pollack, M.S.; Levine, L.S.; Pang, S.;Lancet,1979

3. First trimester prenatal diagnosis of 21-hydroxylase deficicncv by linkagc analysis to HLA-DNA probes and by 17 hydroxyprogesterone determination;Mornet, E.; Boue, J.; Raux-D)emay, M.; Couillion, P.;Hum fenet,1986

4. hita SK, 'I'ynan MJ. Prenatal screening for congenital heart disease;Allan, L.D.; Crawford, D.C.,1986

5. P'redictive value, sensitivity, and specificity of ultrasonic targcted imaging for fetal anomalies in gravid women at high risk for birth def'ects;true;Am]fObstet fGsnecol,1985

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1. Non-Invasive Prenatal Diagnosis Using Cell-Free Fetal DNA Technology: Applications and Implications;Public Health Genomics;2010

2. Obstetrics;Medical Journal of Australia;1994-08

3. PULMONARY DISORDERS COMPLICATING PREGNANCY;Obstetrics and Gynecology Clinics of North America;1992-12

4. Costs and Benefits of Prenatal Screening for Cystic Fibrosis;Medical Care;1991-05

5. Developments in the new genetics*;Journal of Public Health;1990-02

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