An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methods-Reference-Cited by-同舟云学术

An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methods

Published:1991-04 Issue:1 Tuberous Scle Volume:615 Page:298-305
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:Ann NY Acad Sci

Author:

POVEY S.,ATTWOOD J.,JANSSEN L. A. J.,BURLEY M.,SMITH M.,FLODMAN P.,MORTON N. E.,EDWARDS J. H.,SAMPSON J. R.,YATES J. R. W.,HAINES J. L.,AMOS J.,SHORT M. P.,SANDKUYL L. A.,HALLEY D. J. J.,FRYER A. E.,BECH-HANSEN T.,MUELLER R.,AL-GHAZALI L.,SUPER M.,OSBORNE J.

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1991.tb37771.x/fullpdf

Reference13 articles.

1. OSTEOGENESIS IMPERFECTA IS LINKED TO BOTH TYPE I COLLAGEN STRUCTURAL GENES

2. 3. L. A. J. Janssen, S. Povey, J. Attwood, L. A. Sandkuyl, D. Lindhout, P. Flodman, M. Smith, J. R. Sampson, J. L. Haines, E. C. Merkens, P. Fleury, and D. J. J. Halley, 1990 . A comparative study on genetic heterogeneity in tuberous sclerosis: Evidence for one gene on 9q34 and a second gene on 11q22-23. Ann. N.Y. Acad. Sci.

3. EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

4. GENETIC RECOMBINATION BETWEEN TUBEROUS SCLEROSIS AND ONCOGENE v-abl

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1. Tuberous Sclerosis: Between Genetic and Physical Analysis;Acta geneticae medicae et gemellologiae: twin research;1996-04

2. Novel Mutations Detected in the TSC2 Hene From Both Sporadic and Familial TSC Patients;Human Molecular Genetics;1996-02

3. Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex.;Journal of Medical Genetics;1996-01-01

4. Clinical, Neuropathological and Genetic Aspects of the Tuberous Sclerosis Complex;Brain Pathology;1995-04

5. Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13;Annals of Human Genetics;1994-05