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1
Recurrence of duchenne dystrophy through non-maternal lines in four genealogies
Recurrence of duchenne dystrophy through non-maternal lines in four genealogies
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Recurrence of duchenne dystrophy through non-maternal lines in four genealogies

Mayana Zatz Maria Rita Passos-Bueno; D Rapaport; Mariz Vainzof; International Congress of Neuromuscular Diseases (7. 1990 Munich)

Abstracts 1990

Munich 1990

Item não circula. Consulte sua biblioteca.(Acessar)

2
X-autosome translocations in females with X-linked recessive diseases
X-autosome translocations in females with X-linked recessive diseases
Material Type:
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X-autosome translocations in females with X-linked recessive diseases

Angela M Vianna-Morgante D A S Batista; R Levisky; Mayana Zatz; International Congress of Human Genetics (7. 1986 Berlin)

Abstracts 1986

Berlin 1986

Item não circula. Consulte sua biblioteca.(Acessar)

3
Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation
Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation

D Rapaport Maria Rita Passos-Bueno; L Brandao; M Vainzof; M A B O Lima; M Zatz; International Congress on Neuromuscular Diseases (7. 1990 Munich)

Abstracts 1990

Munich 1990

Item não circula. Consulte sua biblioteca.(Acessar)

4
Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies
Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies

Mariz Vainzof R C M Pavanello; D Rapaport; Maria Rita Passos-Bueno; E E Zubrzycka-Gaarn; E Hoffman; Mayana Zatz; International Congress on Neuromuscular Diseases (7. 1990 Munich)

Abstracts 1990

Munich 1990

Item não circula. Consulte sua biblioteca.(Acessar)

5
Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b)
Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b)

L Mahjneh Maria Rita Passos-Bueno; M Zatz; M Vainzof; G Marconi; L Nashef; R Bashir; K Bushby; Limb Girdle Muscular Dystrophies Genetics Workshop (1996 Tunis)

Abstracts 1996

Tunis 1996

Item não circula. Consulte sua biblioteca.(Acessar)

6
Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)
Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)
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Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)

Maria Rita Passos-Bueno D Love; B Byth; J Terwillinger; D Rapaport; K E Davies; Mayana Zatz; International Congress on Neuromuscular Diseases (7. 1990 Munich)

Abstracts 1990

Munich 1990

Item não circula. Consulte sua biblioteca.(Acessar)

7
Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b)
Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b)
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Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b)

K Bushby R Bashir; S Britton; S Keers; I Mahjneh; M Zatz; T Strachan; Limb Girdle Muscular Dystrophies Genetics Workshop (1996 Tunis)

Abstracts 1996

Tunis 1996

Item não circula. Consulte sua biblioteca.(Acessar)

8
Gender differences in the genetic determinants to alcohol dependence
Gender differences in the genetic determinants to alcohol dependence
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Gender differences in the genetic determinants to alcohol dependence

Mayana Zatz Camila Guindalini; Sandra Scivoletto; R. G. M Ferreira; A Nishimura; M Ziberman; Marco Aurélio Peluso; Annual Meeting of the American Society of Human Genetics (52. 2002 Baltimore)

Abstracts v. 71, n. 4, suppl., p. 471 res.1763, oct. 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

9
Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients?
Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients?
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients?

Dulci do Nascimento Fonseca Vagenas A M P Cerqueira; A Torres; Rita de Cássia M Pavanello; Maria Rita Passos-Bueno; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (52. 2002 Baltimore)

Abstracts v. 71, n. 4, suppl., p. 525 res.2083, oct. 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

10
Another locus for autosomal dominant late onset Alzheimers disease in brazilian families?
Another locus for autosomal dominant late onset Alzheimers disease in brazilian families?
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Another locus for autosomal dominant late onset Alzheimers disease in brazilian families?

A. L. Nishimura J. R. M Oliveira; Paulo Roberto Brito-Marques; Ricardo Nitrini; P. H Bertolucci; Ivan H Okamoto; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (52. 2002 Baltimore)

Abstracts v. 71, n. 4, suppl. p. 480 res.1814, 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Zatz, R
  2. Zatz, M
  3. International Congress of Nephrology
  4. Passos-Bueno, M
  5. Santos, M

Neste Assunto:

  1. Genética Médica
  2. Nefrologia
  3. Idosos
  4. Ratos
  5. Doenças Genéticas

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

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