Literature DB >> 3139178

Prenatal diagnosis of common genetic disorders.

M D Crawfurd1.   

Abstract

Entities:  

Mesh：

Year:  1988        PMID： 3139178      PMCID： PMC1840345          DOI： 10.1136/bmj.297.6647.502

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  60 in total

1.  First trimester chorionic villus sampling versus mid-trimester genetic amniocentesis--preliminary results of a controlled prospective trial.

Authors:  J P Crane; H A Beaver; S W Cheung
Journal:  Prenat Diagn       Date:  1988-06       Impact factor: 3.050

2.  Screening programme for prevention of Down's syndrome.

Authors:  Z Stein; M Susser; A V Guterman
Journal:  Lancet       Date:  1973-02-10       Impact factor: 79.321

3.  Antenatal diagnosis of sickle cell anemia by sensitive DNA assay.

Authors:  J C Chang; M S Golbus; Y W Kan
Journal:  Lancet       Date:  1982-06-26       Impact factor: 79.321

4.  Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiency.

Authors:  C H Rodeck; A D Patrick; M E Pembrey; C Tzannatos; A E Whitfield
Journal:  Lancet       Date:  1982-08-07       Impact factor: 79.321

5.  Same-day, first-trimester antenatal diagnosis for cystic fibrosis by gene amplification.

Authors:  C Williams; R Williamson; C Coutelle; F Loeffler; J Smith; A Ivinson
Journal:  Lancet       Date:  1988-07-09       Impact factor: 79.321

6.  Ultrasound in the diagnosis of spina bifida.

Authors:  S Campbell; J Pryse-Davies; T M Coltart; M J Seller; J D Singer
Journal:  Lancet       Date:  1975-05-10       Impact factor: 79.321

7.  Marker X chromosomes, mental retardation and macro-orchidism.

Authors:  G Turner; R Till; A Daniel
Journal:  N Engl J Med       Date:  1978-12-28       Impact factor: 91.245

8.  Obstetric outcome and problems of mid-trimester fetal blood sampling for antenatal diagnosis.

Authors:  R H Ward; B Modell; D V Fairweather; I M Shirley; B A Richards; C P Hetherington
Journal:  Br J Obstet Gynaecol       Date:  1981-11

9.  Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.

Authors:  M S Pollack; D Maurer; L S Levine; M I New; S Pang; M Duchon; R P Owens; I R Merkatz; B M Nitowsky; G Sachs; B Dupont
Journal:  Lancet       Date:  1979-05-26       Impact factor: 79.321

10.  Reactivity of amniotic fluid alpha-fetoprotein with concanavallin A in diagnosis of neural tube defects.

Authors:  C J Smith; P C Kelleher; L Bélanger; L Dallaire
Journal:  Br Med J       Date:  1979-04-07
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  1 in total

Review 1.  Advances in the study of inherited metabolic disease.

Authors:  D A Gibbs
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982
  1 in total

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