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1
Autosomal dominant pure spastic paraplegia in a brazilian family linkage to chromosome 8q and study of muscle syntrophin 'beta'1
Autosomal dominant pure spastic paraplegia in a brazilian family linkage to chromosome 8q and study of muscle syntrophin 'beta'1
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Autosomal dominant pure spastic paraplegia in a brazilian family linkage to chromosome 8q and study of muscle syntrophin 'beta'1

P S Rocco Mariz Vainzof; S C Froehner; Suely Kazue Nagahashi Marie; Louis M Kunkel; Maria Rita Passos-Bueno; Mayana Zatz; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res.2508, oct., 1999

San Francisco 1999

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2
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
Material Type:
Artículo 		Añadir a Mi Portal

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12

E S Moreira M Vainzof; Suely Kazue Nagahashi Marie; A L Sertie; M Zatz; Maria Rita Passos-Bueno

Baltimore v. 61, p. 151-159, 1997 American Journal of Human Genetics

Baltimore 1997

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3
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
Material Type:
Artículo 		Añadir a Mi Portal

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12

E S Moreira Mariz Vainzof; Suely Kazue Nagahashi Marie; A L Sertie; Mayana Zatz; Maria Rita Passos-Bueno

Baltimore v. 61, p. 151-159, 1997 American Journal of Human Genetics

Baltimore 1997

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4
Linkage analysis in a large brazilian family with knobloch syndrome
Linkage analysis in a large brazilian family with knobloch syndrome
Material Type:
Artículo de Congreso 		Añadir a Mi Portal

Linkage analysis in a large brazilian family with knobloch syndrome

Maria Rita Passos-Bueno A L Sertie; M Quimby; J Murray; Suely Kazue Nagahashi Marie; M Zatz; Annual Meeting of the American Society of Human Genetics (45. 1995 Minneapolis)

v.57, n.4 suppl., p.a333, oct. 1995 American Journal of Human Genetics

1995

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5
High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
Material Type:
Artículo 		Añadir a Mi Portal

High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families

M Zatz Suely Kazue Nagahashi Marie; Maria Rita Passos-Bueno; M Vainzof; S Campiotto; A M P Cerqueira; C Wijmenga; G Padberg; R Frants

Baltimore v.56, n.1 , p.99-105, jan. 1995 American Journal of Human Genetics

Baltimore 1995

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6
High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
Material Type:
Artículo 		Añadir a Mi Portal

High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families

Mayana Zatz Suely Kazue Nagahashi Marie; Maria Rita Passos-Bueno; Mariz Vainzof; S Campiotto; A M P Cerqueira; C Wijmenga; G Padberg; R Frants

Baltimore v.56, n.1 , p.99-105, jan. 1995 American Journal of Human Genetics

Baltimore 1995

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por este autor/creador:

  1. Passos-Bueno, M
  2. Marie, S
  3. Zatz, M
  4. Vainzof, M
  5. Sertie, A

con este tema:

  1. Genética Médica

  • Realización: ABCD-USP USP   Logos de Redes Sociales: Freepik

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