Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.-Reference-Cited by-同舟云学术

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.

Published:1996-01-01 Issue:1 Volume:33 Page:29-35
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bakker E,Van der Wielen M J,Voorhoeve E,Ippel P F,Padberg G W,Frants R R,Wijmenga C

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Facioscapulohunmeral disease;Padberg, G.W.,1982

2. Estimation of age ddyespternodpehnytbpyemnientirmainscienginasfcaecritoasicnampeunltohbuimase.ra3lMmeudscGuelnaert;Lunt, P.W.; Compston, D.A.; Harper, P.S.,1989

3. Job perspectives in facioscapulohumeral muscular dystrophy;Wevers, C.W.J.; Brouwer, O.F.; Padberg, G.W.; Nijboer, I.D.;Dis Rehabil,1993

4. Localisation of fasioscapulohumeral muscular dystrophy gene on chromosome 4;Wijmenga, C.; Frants, R.R.; Brouwer, O.F.; Moerer, P.; Weber, J.; Padberg, G.W.;Lancet,1990

5. Mapping the facioscapulohumeral muscular dystrophy gene is complicated by 4q35 recombination events;Weiffenbach, B.; Dubois, J.; Storvick, D.;ANature Genet,1993

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