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PMID: 3545058 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Fragile X syndrome: a unique mutation in man.

Annual review of genetics ·Vol. 20 ·1986-00-00 ·Pages 109-45

Nussbaum RL, Ledbetter DH

Abstract

暂无摘要

MeSH Terms

Caffeine/pharmacology Chromosome Fragility/drug effects Female Fragile X Syndrome/genetics Genetic Counseling Genetic Linkage Genetic Markers Heterozygote Humans Hybrid Cells/ultrastructure Intellectual Disability/genetics Male Methotrexate/pharmacology Models, Genetic Pedigree Phenotype Sex Chromosome Aberrations/genetics Thymidine/physiology

Chemicals

Genetic Markers Caffeine Thymidine Methotrexate

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Nussbaum R L

Ledbetter D H

Article Info

Journal

Annual review of genetics

Abbr.

Annu Rev Genet

ISSN

0066-4197

DOI

10.1146/annurev.ge.20.120186.000545

Published

1986-00-00

Pages

109-45

Language

English

Region

United States

NLM ID

0117605

Subset

External Links

PubMed source DOI: 10.1146/annurev.ge.20.120186.000545 View journal details

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