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1
Genetics of leydig cell hypoplasia
Genetics of leydig cell hypoplasia
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Genetics of leydig cell hypoplasia

P H N Saldanha S. P. A Toledo (Sérgio Pereira de Almeida); International Congress of Human Genetics (7. 1986 Berlin)

Abstracts 1986

Berlin 1986

Item não circula. Consulte sua biblioteca.(Acessar)

2
Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)
Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

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)

3
Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b)
Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b)
Material Type:
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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)

4
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)

5
Familial leyding cell clc hypoplasia without genital malformation
Familial leyding cell clc hypoplasia without genital malformation
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Familial leyding cell clc hypoplasia without genital malformation

S. P. A. Toledo (Sérgio Pereira de Almeida) I J P Arnold; W Luthold; E M K Russo; P H N Saldanha; International Congress of Human Genetics (7. 1986 Berlin)

Abstracts 1986

Berlin 1986

Item não circula. Consulte sua biblioteca.(Acessar)

6
Inherited homozygous paracentric inversion affecting both arms of chromosome 12
Inherited homozygous paracentric inversion affecting both arms of chromosome 12
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Inherited homozygous paracentric inversion affecting both arms of chromosome 12

Lúcia Regina Martelli I Gomy; L. A. F Laureano; M Yoshimoto; Ester Silveira Ramos; M. S. J. de Vozzi; J. A Squire; Annual Meeting of the American Society of Human Genetics (ASHG) (57. 2007 San Diego)

Abstracts San Diego, 2007

San Diego 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1643519 ) e outros locais(Acessar)

7
Six autosomal recessive limb-girdle muscular dystrophies in brazil
Six autosomal recessive limb-girdle muscular dystrophies in brazil
Material Type:
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Six autosomal recessive limb-girdle muscular dystrophies in brazil

M Zatz M Vainzof; E S Moreira; Suely Kazue Nagahashi Marie; K Bushby; L Anderson; C G Bonnemann; E M Mcnally; V Nigro; L M Kunkel; Maria Rita Passos-Bueno; Limb Girdle Muscular Dystrophies Genetics Workshop (1996 Tunis)

Abstracts 1996

Tunis 1996

Item não circula. Consulte sua biblioteca.(Acessar)

8
Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b)
Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

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)

9
Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother a clinical and pathological study
Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother a clinical and pathological study
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother a clinical and pathological study

A Richieri-Costa U Frederique Junior; Maria Leine Guion-Almeida; International Workshop on Fetal Genetic Pathology (2. 1991 Montana)

Abstracts Montana : Shodair Children S Hospital, 1991

Montana Shodair Children S Hospital 1991

Item não circula. Consulte sua biblioteca.(Acessar)

10
Analysis of ETV6/Runx fusions for evaluating the late effects of cancer thereapy in all (acute lymphoblistic leukemia)cured patients
Analysis of ETV6/Runx fusions for evaluating the late effects of cancer thereapy in all (acute lymphoblistic leukemia)cured patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analysis of ETV6/Runx fusions for evaluating the late effects of cancer thereapy in all (acute lymphoblistic leukemia)cured patients

Maria Sol Brassesco Marjori Leiva Camparoto; Luiz Gonzaga Tone; Elza Tiemi Sakamoto-Hojo; International Symposium on Chromosomal Aberrations (ISCA (2003 Essen)

Abstracts Essen : University of Duisburg, 2003

Essen University of Duisburg 2003

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1351080 ) e outros locais(Acessar)

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