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1
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies

M Vainzof Maria Rita Passos-Bueno; N Man; M Zatz

New York v.58, n.4 , p.305-9, 1995 American Journal of Medical Genetics

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

2
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies

Mariz Vainzof Maria Rita Passos-Bueno; N Man; Mayana Zatz

New York v.58, n.4 , p.305-9, 1995 American Journal of Medical Genetics

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

3
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers

Denilce Ritsuko Sumita Mariz Vainzof; Simone Campiotto; Antonia M Cerqueira; Marta Canovas; Paulo A Otto; Maria Rita Passos-Bueno; Mayana Zatz

American Journal of Medical Genetics v. 80, p. 356-361, 1998

New York 1998

Item não circula. Consulte sua biblioteca.(Acessar)

4
Additional dystrophin fragment in Becker muscular dystrophy patients correlation with the pattern DNA deletion. [Carta ao editor]
Additional dystrophin fragment in Becker muscular dystrophy patients correlation with the pattern DNA deletion. [Carta ao editor]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Additional dystrophin fragment in Becker muscular dystrophy patients correlation with the pattern DNA deletion. [Carta ao editor]

Mariz Vainzof Maria Rita Passos-Bueno; Debora Rapaport; Rita de Cássia M Pavanello; Mayana Zatz; Dennis E Bulman

American Journal of Medical Genetics v. 44, n. 3, p. 382-384, 1992

New York 1992

Item não circula. Consulte sua biblioteca.(Acessar)

5
Additional dystrophin fragment in Becker muscular dystrophy patients correlation with the pattern DNA deletion. [Carta ao editor]
Additional dystrophin fragment in Becker muscular dystrophy patients correlation with the pattern DNA deletion. [Carta ao editor]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Additional dystrophin fragment in Becker muscular dystrophy patients correlation with the pattern DNA deletion. [Carta ao editor]

Mariz Vainzof Maria Rita Passos-Bueno; Debora Rapaport; Rita de Cássia M Pavanello; Mayana Zatz; Dennis E Bulman

American Journal of Medical Genetics v. 44, n. 3, p. 382-384, 1992

New York 1992

Item não circula. Consulte sua biblioteca.(Acessar)

6
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis

Mayana Zatz Paulo A Otto

New York v.25, n.2 , p.219-31, 1986 American Journal of Medical Genetics

New York 1986

Item não circula. Consulte sua biblioteca.(Acessar)

7
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis

Mayana Zatz Paulo Alberto Otto

New York v.25, n.2 , p.219-31, 1986 American Journal of Medical Genetics

New York 1986

Item não circula. Consulte sua biblioteca.(Acessar)

8
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology

Klaus Zerres Gabi Mücher; Jutta Becker; Carsten Steinkmamm; Sabine Rudnik Schöneborn; Päivi Heikkilä; Juhani Rapola; Riitta Salonen; Gregory G Germino; Luiz Fernando Onuchic; Stefan Somlo; Ellis D Avner; Leight A Harman; John M Stockwin; Lisa M. Guay Woodford

American Journal of Medical Genetics v. 76, n. 02, p. 137-144, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

9
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology

Klaus Zerres Gabi Mücher; Jutta Becker; Carsten Steinkmamm; Sabine Rudnik Schöneborn; Päivi Heikkilä; Juhani Rapola; Riitta Salonen; Gregory G Germino; Luiz Fernando Onuchic; Stefan Somlo; Ellis D Avner; Leight A Harman; John M Stockwin; Lisa M. Guay Woodford

American Journal of Medical Genetics v. 76, n. 02, p. 137-144, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Zatz, M
  2. Vainzof, M
  3. Passos-Bueno, M
  4. Otto, P
  5. Becker, J

Neste Assunto:

  1. Distrofia Muscular
  2. Genética Médica
  3. Doenças Genéticas
  4. Medicina Interna
  5. Genética

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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