Literature DB >> 856956

Rapid prenatal diagnosis of the Lesch-Nyhan syndrome.

D Halley, M J Heukels-Dully.   

Abstract

Autoradiographic demonstration of 3H-hypoxanthine incorporation in small numbers of amniotic fluid cells cultured on coverslips is a rapid and practical technique in the prenatal diagnosis of the Lesch-Nyhan mutation. An affected male fetus, a normal male fetus, and a heterozygous female fetus were identified within 14 days after amniocentesis in three pregancies at risk for the Lesch-Nyhan syndrome.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 856956      PMCID: PMC1013522          DOI: 10.1136/jmg.14.2.100

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  6 in total

1.  Biochemical diagnosis of an X-linked disease in utero.

Authors:  W Y Fujimoto; J E Seegmiller; B W Uhlendorf; C B Jacobson
Journal:  Lancet       Date:  1968-08-31       Impact factor: 79.321

2.  Rapid tissue culture and microbiochemical methods for analyzing colonially grown fibroblasts from normal, Lesch-Nyhan and Tay-Sachs patients and amniotic fluid cells.

Authors:  B J Richardson; D M Cox
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

3.  Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases.

Authors:  M F Niermeijer; D Halley; E Sachs; C Tichelaar-Klepper; K L Garver
Journal:  Humangenetik       Date:  1973

4.  Preventive control of the Lesch-Nyhan syndrome.

Authors:  P J Van Heeswijk; C H Blank; J E Seegmiller; C B Jacobson
Journal:  Obstet Gynecol       Date:  1972-07       Impact factor: 7.661

5.  Lesch-Nyhan syndrome: preventive control by prenatal diagnosis.

Authors:  J A Boyle; K O Raivio; K H Astrin; J D Schulman; M L Graf; J E Seegmiller; C B Jacobsen
Journal:  Science       Date:  1970-08-14       Impact factor: 47.728

6.  Rapid determination of hypoxanthine-guanine-phosphoribosyl transferase in human fibroblasts and amniotic cells.

Authors:  I Willers; D P Agarwal; S Singh; W Schloot; H W Goedde
Journal:  Humangenetik       Date:  1975
  6 in total
  2 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

2.  Family studies of the Lesch-Nyhan syndrome: the use of a restriction fragment length polymorphism (RFLP) closely linked to the disease gene for carrier state and prenatal diagnosis.

Authors:  D A Gibbs; C M Headhouse-Benson; R W Watts
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.