Genetics of Facioscapulohumeral Dystrophy

J Gordon Millichap

doi:10.15844/pedneurbriefs-10-8-3

Genetics of Facioscapulohumeral Dystrophy

Pediatric Neurology Briefs

Volume 10 (1996): Issue 8

By: J Gordon Millichap

Open Access

|Aug 1996

Abstract

The relationship of phenotype to genotype in a clinically and genetically well defined population of 157 affected patients and 62 kindreds with facioscapulohumeral muscular dystrophy (FSHD) was examined at the University of Rochester School of Medicine, NY, and Ohio State University, Columbus, OH.

References

Tawil R Forrester J Griggs RC Mendell J Kissel J McDermott M Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy Ann Neurol 1996 Jun 39 6 744 748 10.1002/ana.410390610 8651646
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Ueyama H Kumamoto T Mita S Kimura E Nakagawa M Uchino M Facioscapulohumeral muscular dystrophy with chromosome 9p deletion Neurology 1996 Feb 46 2 566 569 10.1212/WNL.46.2.566 8614537
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-10-8-3 | Journal eISSN: 2166-6482

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Language: English

Page range: 58 - 59

Published on: Aug 1, 1996

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Facioscapulohumeral Muscular Dystrophy,

Isometric Myometry Scores,

Trigonocephaly

© 1996 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 10 (1996): Issue 8