First trimester diagnosis of lesch-nyhan syndrome: Applications to other disorders of purine metabolism-Reference-Cited by-同舟云学术

First trimester diagnosis of lesch-nyhan syndrome: Applications to other disorders of purine metabolism

Published:1985-05 Issue:3 Volume:5 Page:183-189
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Stout J. Timothy,Jackson Laird G.,Caskey C. Thomas

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference9 articles.

1. (1985). Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in the region Xq26 qter, Somatic Cell and Mol. Gen., in press.

2. (1985). Antenatal diagnosis of neurological disorders. In: (Ed.). Pediatric Neurology, New York: Grune and Stratton, in press.

3. A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PRENATAL DIAGNOSIS BY ENZYME ANALYSIS IN 15 PREGNANCIES AT RISK FOR THE LESCH–NYHAN SYNDROME;Prenatal Diagnosis;1996-07

2. Prenatal Diagnosis of Lesch-Nyhan Syndrome;Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism;1993

3. Prenatal diagnosis of Lesch-Nyhan syndrome: Experience with three fetuses at risk;Prenatal Diagnosis;1989-09

4. Failure to diagnose Lesch-Nyhan syndrome by first trimester chorionic villus sampling;Prenatal Diagnosis;1989-06

5. Prenatal diagnosis of purine nucleoside phosphorylase deficiency in the first and second trimesters of pregnancy;Prenatal Diagnosis;1989-06