POLYMORPHIC DNA MARKERS IN PRENATAL DIAGNOSIS OF FRAGILE X SYNDROME-Reference-Cited by-同舟云学术

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POLYMORPHIC DNA MARKERS IN PRENATAL DIAGNOSIS OF FRAGILE X SYNDROME

Published:1985-04 Issue:8433 Volume:325 Page:871
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Oberle I,Mandel J.L,Boué J,Mattei M.G,Mattei J.F

Publisher

Elsevier BV

Subject

General Medicine

Reference10 articles.

1. Feasibility of fraX chromosome prenatal diagnosis demonstrated;Jenkins;Lancet,1981

2. Prenatal diagnosis of Martin-Bell syndrome associated with fragile site at Xq27-28;Webb;Lancet,1981

3. First trimester prenatal diagnosis of a male fetus with fragile X;Tommerup;Lancet,1985

4. Oberlé I, Heilig R, Moisan JP, et al Genetic analysis of the fragile X mental retardation syndrome with two flanking polymorphic DNA markers. Unpublished.

5. Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus);Camerino;Proc Natl Acad Sci (USA),1984

Cited by 29 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. Pulsed-Field Gel Electrophoresis and the Molecular Epidemiology of Foodborne Pathogens;DNA Methods in Food Safety;2014-08-29

2. A faster strategy for prenatal diagnosis of fragile X syndrome;Prenatal Diagnosis;2010-09-13

3. Diagnostic molecular genetics of the fragile X;Clinical Genetics;2008-06-28

4. The fragile X chromosome: prenatal diagnosis;Clinical Genetics;2008-04-23

5. DNA DIAGNOSIS FOR THE PRACTICING OBSTETRICIAN;Obstetrics and Gynecology Clinics of North America;1997-03

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