Fragile X—A Family of Disorders: Changing Phenotype and Molecular Genetics-Reference-Cited by-同舟云学术

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Fragile X—A Family of Disorders: Changing Phenotype and Molecular Genetics

Published:2012-08-30 Issue: Volume: Page:453-471
ISSN:
Container-title:The Principles of Clinical Cytogenetics
language:
Short-container-title:

Author:

Spector Elaine B.

Publisher

Springer New York

Link

http://link.springer.com/content/pdf/10.1007/978-1-4419-1688-4_19

Reference194 articles.

1. Penrose LS. A clinical and genetic study of 1,280 cases of mental defect. Special report series no. 229. London: Medical Research Council; 1938.

2. Howard-Peebles PN. Non-specific X-linked mental retardation: background, types, diagnosis and prevalence. J Ment Defic Res. 1982;26:205–13.

3. Lubs HA. A marker X chromosome. Am J Hum Genet. 1969;21:231–44.

4. Hamel BCJ, Chiurazzi P, Lubs HA. Syndromic XLMR genes (MRXS): update 2000. Am J Med Genet. 2000;94:361–3.

5. Martin JP, Bell J. A pedigree of mental defect showing sex-linkage. J Neurol Psychiatry. 1943;6:154–7.

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