Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.-Reference-Cited by-同舟云学术

Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

Published:1987-01-01 Issue:1 Volume:24 Page:14-22
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Connor J M,Pirrit L A,Yates J R,Crossley J A,Imrie S J,Colgan J M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference37 articles.

1. Screening for fra(X) (q) in a population of mentally retarded males;Froster-Iskenius, U.; Felsch, G.; Schhirren, C.; Schwinger, E.;Hum Genet,1983

2. The fragile X syndrome. A study of 83 families;Fryns, J.P.;Clin Genet,1984

3. The fragile X syndrome: the patients and their chromosomes;MA, De Arce; A, Kearns;i Med Genet,1984

4. Marker (X)-linked mental retardation;Turner, G.; Jacobs, P.A.;Adv Hum Genet,1983

5. Conference report. International workshop on the fragile X and X-linked mental retardation;Opitz, J.M.; Sutherland, G.R.;Am J Med Genet,1984

Cited by 11 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. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms;Cytogenetic and Genome Research;1991

3. Report of the committee on the genetic constitution of the X chromosome;Cytogenetic and Genome Research;1991

4. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991

5. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms;Cytogenetic and Genome Research;1990