Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families
Maria Rita Passos-Bueno C Wijmenga; R I Takata; Suely Kazue Nagahashi Marie; M Vainzof; R C M Pavanello; J E Hewitt; E Bakker; A A S Carvalho; J Akiyama; R R Frants; World Congress of Neurology (15. 1993 Vancouver)
Calgary v.20, n.suppl.4, p.s30, aug. 1993 Canadian Journal of Neurological Sciences
Calgary 1993
Localização:
FM - Fac. Medicina
(BCSEP 1993 038 ) e outros locais(Acessar)
Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
Maria Rita Passos-Bueno E S Moreira; Mariz Vainzof; L Pereira; Suely Kazue Nagahashi Marie; J Akiyama; Mayana Zatz; Congresso Nacional de Genetica (41. 1995 Caxambu)
v.13, n.3 suppl., p.557, sep. 1995 Revista Brasileira de Genetica = Brazilian Journal of Genetics
1995
Item não circula. Consulte sua biblioteca.(Acessar)
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Maria Rita Passos-Bueno E S Moreira; Mariz Vainzof; J Chamberlain; Suely Kazue Nagahashi Marie; L Pereira; J Akiyama; S L Roberds; K P Campbell; Mayana Zatz
Oxford v.4 , n.7 , p.1163-7, 1995 Human Molecular Genetics
Oxford 1995
Item não circula. Consulte sua biblioteca.(Acessar)
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Maria Rita Passos-Bueno E S Moreira; M Vainzof; J Chamberlain; Suely Kazue Nagahashi Marie; L Pereira; J Akiyama; S L Roberds; K P Campbell; M Zatz
Oxford v.4 , n.7 , p.1163-7, 1995 Human Molecular Genetics
Oxford 1995
Item não circula. Consulte sua biblioteca.(Acessar)
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
Maria Rita Passos-Bueno C Wijmenga; R I Takata; Suely Kazue Nagahashi Marie; Mariz Vainzof; R C M Pavanello; J E Hewitt; E Bakker; A Carvalho; J Akiyama; R R Frants
Oxford v.2 , n.5 , p.557-62, 1993 Human Molecular Genetics
Oxford 1993
Item não circula. Consulte sua biblioteca.(Acessar)