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1
Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families
Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

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

Disponible en FM - Fac. Medicina    (BCSEP 1993 038 ) y otras localizaciones(Obténgalo)

2
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
Material Type:
Artículo 		Añadir a Mi Portal

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

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3
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families
Material Type:
Artículo 		Añadir a Mi Portal

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families

Maria Rita Passos-Bueno I Richard; M Vainzof; F Fougerousse; J Weissenbach; O Broux; D Cohen; J Akiyama; Suely Kazue Nagahashi Marie; A. A Carvalho; L Guilherme

London v.30, n.5 , p.385-7, 1993 Journal of Medical Genetics

London 1993

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4
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
Material Type:
Artículo 		Añadir a Mi Portal

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; M 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

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5
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families
Material Type:
Artículo 		Añadir a Mi Portal

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families

Maria Rita Passos-Bueno I Richard; Mariz Vainzof; F Fougerousse; J Weissenbach; O Broux; D Cohen; J Akiyama; Suely Kazue Nagahashi Marie; A. A Carvalho; L Guilherme

London v.30, n.5 , p.385-7, 1993 Journal of Medical Genetics

London 1993

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6
Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

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

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7
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Material Type:
Artículo 		Añadir a Mi Portal

Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study

M. Melo V Lauriano; V Gentil; S Eggers; S S Bianco; P R Gimenez; J Akiyama; H Okabaiashi; O Frota-Pessoa; Maria Rita Passos-Bueno; Mayana Zatz

New York v.60, n.1 , p.33-8, feb. 1995 American Journal of Medical Genetics (Neuropsychiatric Genetics)

New York 1995

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8
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Material Type:
Artículo 		Añadir a Mi Portal

Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study

M. Melo V Lauriano; V Gentil; S Eggers; S S Bianco; P R Gimenez; J Akiyama; H Okabaiashi; O Frota-Pessoa; Maria Rita Passos-Bueno; M Zatz

New York v.60, n.1 , p.33-8, feb. 1995 American Journal of Medical Genetics (Neuropsychiatric Genetics)

New York 1995

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9
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Material Type:
Artículo 		Añadir a Mi Portal

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

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10
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Material Type:
Artículo 		Añadir a Mi Portal

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

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por este autor/creador:

  1. Passos-Bueno, M
  2. Akiyama, J
  3. Vainzof, M
  4. Marie, S
  5. Zatz, M

con este tema:

  1. Genética Médica
  2. Surdez
  3. Crianças
  4. Família
  5. Pintura

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