Association of schizophrenia and becker muscular dystrophy (bmd) a susceptibility locus for schizophrenia in xp21 or an effect of the dystrophin gene in the brain?
Mayana Zatz M S Melo; H P Vallada; Maria Rita Passos-Bueno; A. H. G Vieira Filho; Mariz Vainzof; D Rapaport; Valentim Gentil Filho; World Congress on Psychiatric Genetics (2. 1991 Cambridge)
v.2 , n.1 , p.101-2, 1991 Psychiatric Genetics
1991
Localização:
FM - Fac. Medicina
(BCSEP 1991 041 ) e outros locais(Acessar)
Possible digenic for limb girdle muscular dystropy
Alessandra Starling F de Paula; Rita de Cássia M Pavanello; Mariz Vainzof; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)
American Journal of Human Genetics Baltimore v. 73, n. 5, suppl., p. 481, 2003
Baltimore 2003
Item não circula. Consulte sua biblioteca.(Acessar)
Novel dysferlin mutations in brazilian LGMD2B patients
F. Paula Mariz Vainzof; E. S Moreira; Maria Rita Passos-Bueno; K Bushby; Rumaisa Bashir; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)
American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 639, oct. 2001
Chicago 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Evidence of further genetic heterogeneity for both autosomal dominant and autosomal recessive limb-girdle muscular dystrophy
A. L. Starling Mariz Vainzof; Rita de Cássia M Pavanello; M Canovas; A Cerqueira; Maria Rita Passos-Bueno; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)
American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 513, oct. 2001
Chicago 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Muscle proteins alteration in patients with mutations in the Fukutin-Related protein gene
L. U. Yamamoto Marta Canovas; Rita de Cássia M Pavanello; B. L Lima; F de Paula; N Vieira; Mayana Zatz; Mariz Vainzof; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)
American Journal of Human Genetics Baltimore v. 73, n. 5, suppl., p. 556, 2003
2003
Item não circula. Consulte sua biblioteca.(Acessar)
Mariz Vainzof Georgine Faulkner; G Valle; A Beggs; O Carpen; P Salmikangas; C Wallgren-Pettersson; Siegfried Labeit; Juliana Gurgel-Gianneti; E. S Moreira; Maria Rita Passos-Bueno; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)
American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 638, oct. 2001
Chicago 2001
Item não circula. Consulte sua biblioteca.(Acessar)
'BETA'-sarcoglycan mutations in severe limb-girdle muscular dystrophy type 2e in brazil
C G Bonnemann Maria Rita Passos-Bueno; E M Mcnally; M Vainzof; E S Moreira; S Noguchi; E Ozawa; M Zatz; L M Kunkel; Annual Meeting of the American Society of Human Genetics (46. 1996 San Francisco)
v.59, n.4 suppl., p.1434, 1996 American Journal of Human Genetics
1996
Item não circula. Consulte sua biblioteca.(Acessar)
Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd)
Mariz Vainzof Maria Rita Passos-Bueno; E S Moreira; C G Bonnemann; E M Mcnally; L V B Anderson; V Nigro; L M Kunkel; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (46. 1996 San Francisco)
v.59, n.4 suppl., p.1684, 1996 American Journal of Human Genetics
1996
Item não circula. Consulte sua biblioteca.(Acessar)
Association of schizophrenia and becker dystrophy ( bmd ) a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain
Mayana Zatz M S Melo; Maria Rita Passos-Bueno; H Valada Filho; A. H. G Vieira Filho; Mariz Vainzof; D Rapaport; Valentim Gentil Filho; International Congress of Human Genetics (8. 1991 Washington)
v.49, n.4 suppl., p.364, oct. 1991 American Journal of Human Genetics
1991
Item não circula. Consulte sua biblioteca.(Acessar)
E M Mcnally C G Bonnemann; D Duggan; J R M Gorospe; Maria Rita Passos-Bueno; Mariz Vainzof; Mayana Zatz; S Noguchi; E Ozawa; E P Hoffman; L M Kunkel; Annual Meeting of the American Society of Human Genetics (46. 1996 San Francisco)
v.59, n.4 suppl., p.a271, 1996 American Journal of Human Genetics
1996
Item não circula. Consulte sua biblioteca.(Acessar)