Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): Confirmation of close linkage to D5S39 in French Canadian families
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference18 articles.
1. A PstI polymorphism at the D5S39 locus;Abdelhak;Nucleic Acids Res.,1990
2. Report of the committee on the genetic constitution of chromosome 5;Bishop;Cytogenet. Cell Genet.,1990
3. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2–13.3;Brzustowicz;Nature,1990
4. Report of the committee on methods of linkage analysis and reporting;Conneally;Cytogenet. Cell Genet.,1985
5. Linkage analysis of spinal muscular atrophy;Daniels;Genomics,1992
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4. Enfermedad de Werdnig-Hoffmann. Primer diagnóstico prenatal en Cuba;Revista de Neurología;1999
5. Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number;The American Journal of Human Genetics;1998-12
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