A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA )-Reference-Cited by-同舟云学术

A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA )

Published:1989-12-08 Issue:4935 Volume:246 Page:1298-1300
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Suthers G. K.¹,Callen D. F.¹,Hyland V. J.¹,Kozman H. M.¹,Baker E.¹,Eyre H.¹,Harper P. S.²,Roberts S. H.²,Hors-Cayla M. C.³,Davies K. E.⁴,Bell M. V.⁴,Sutherland G. R.¹

Affiliation:

1. Department of Histopathology, The Adelaide Children's Hospital, North Adelaide SA 5006, Australia.

2. Institute of Medical Genetics, University Hospital of Wales, Cardiff, United Kingdom.

3. Unité de Recherches de Génétique Médicale, Hôpital des Enfants Malades, Paris, France.

4. Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference22 articles.

1. Guide to Molecular Cloning Techniques 1987

2. CALLEN, D.F., A MOUSE-HUMAN HYBRID CELL PANEL FOR MAPPING HUMAN CHROMOSOME-16, ANNALES DE GENETIQUE 29: 235 (1986).

3. CONNEALLY, P.M., REPORT OF THE COMMITTEE ON METHODS OF LINKAGE ANALYSIS AND REPORTING, CYTOGENETICS AND CELL GENETICS 40: 356 (1985).

4. COUTURIER, J, EVIDENCE FOR A CORRELATION BETWEEN LATE REPLICATION AND AUTOSOMAL GENE INACTIVATION IN A FAMILIAL TRANSLOCATION T(X-21), HUMAN GENETICS 49: 319 (1979).

5. DAVIES, K.E., REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF THE X-CHROMOSOMES AND Y-CHROMOSOMES, CYTOGENETICS AND CELL GENETICS 46: 277 (1987).

Cited by 56 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. Forty Years From Markers to Genes;Twin Research and Human Genetics;2008-08-01

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

3. The Pathophysiology of Fragile X Syndrome;Annual Review of Genomics and Human Genetics;2007-09-01

4. A Decade of Molecular Studies of Fragile X Syndrome;Annual Review of Neuroscience;2002-03

5. Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients;Human Genetics;1997-07-09