An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference13 articles.
1. Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).
2. LINKAGE ANALYSIS OF X-LINKED MENTAL RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR IX GENE PROBE
3. The Genetic Distance between the Coagulation Factor IX Gene and the Locus for the Fragile X Syndrome: Clinical Implications
4. Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene
5. The fragile-X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs)
Cited by 21 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. Diagnostic molecular genetics of the fragile X;Clinical Genetics;2008-06-28
2. Cytogenetic experience in prenatal fra(X) detection on amniotic fluid cultures;Prenatal Diagnosis;1992-07
3. Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis;American Journal of Medical Genetics;1992-04-15
4. Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutations;American Journal of Medical Genetics;1991-09-15
5. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304;American Journal of Medical Genetics;1991-02-01
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