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Artigo de periodico
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents (2006)
Rosenberg, Carla ; Knijnenburg, Jeroen; Bakker, E; Vianna-Morgante, Angela M ; Sloos, W.; Otto, Paulo A ; Kriek, M.; Hansson, K.; Krepischi, Ana Cristina Victorino ; Fiegler, H.; Carter, N. P.; Bijlsma, E. K.; Van Haeringen, A.; Szuhai, K.; Tanke, H. J.
Source: Journal of Medical Genetics. Unidade: IB
Subjects: RETARDO MENTAL, DOENÇAS GENÉTICAS
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ABNT
ROSENBERG, Carla et al. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. Journal of Medical Genetics, v. 43, p. 180-186, 2006Tradução . . Disponível em: https://doi.org/10.1136/jmg.2005.032268. Acesso em: 19 set. 2024.
APA
Rosenberg, C., Knijnenburg, J., Bakker, E., Vianna-Morgante, A. M., Sloos, W., Otto, P. A., et al. (2006). Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. Journal of Medical Genetics, 43, 180-186. doi:10.1136/jmg.2005.032268
NLM
Rosenberg C, Knijnenburg J, Bakker E, Vianna-Morgante AM, Sloos W, Otto PA, Kriek M, Hansson K, Krepischi ACV, Fiegler H, Carter NP, Bijlsma EK, Van Haeringen A, Szuhai K, Tanke HJ. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents [Internet]. Journal of Medical Genetics. 2006 ; 43 180-186.[citado 2024 set. 19 ] Available from: https://doi.org/10.1136/jmg.2005.032268
Vancouver
Rosenberg C, Knijnenburg J, Bakker E, Vianna-Morgante AM, Sloos W, Otto PA, Kriek M, Hansson K, Krepischi ACV, Fiegler H, Carter NP, Bijlsma EK, Van Haeringen A, Szuhai K, Tanke HJ. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents [Internet]. Journal of Medical Genetics. 2006 ; 43 180-186.[citado 2024 set. 19 ] Available from: https://doi.org/10.1136/jmg.2005.032268
Artigo de periodico
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization (1998)
Rosenberg, Carla ; Navajas, L; Vagenas, Dulci Fonseca; Bakker, E; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Takata, R I; Van Ommen, G J B; Zatz, Mayana ; Den Dunnen, J T
Source: Neuromuscular Disorders. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ROSENBERG, Carla et al. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization. Neuromuscular Disorders, v. 8, p. 417-452, 1998Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(98)00050-9. Acesso em: 19 set. 2024.
APA
Rosenberg, C., Navajas, L., Vagenas, D. F., Bakker, E., Vainzof, M., Passos-Bueno, M. R., et al. (1998). Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization. Neuromuscular Disorders, 8, 417-452. doi:10.1016/s0960-8966(98)00050-9
NLM
Rosenberg C, Navajas L, Vagenas DF, Bakker E, Vainzof M, Passos-Bueno MR, Takata RI, Van Ommen GJB, Zatz M, Den Dunnen JT. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization [Internet]. Neuromuscular Disorders. 1998 ; 8 417-452.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/s0960-8966(98)00050-9
Vancouver
Rosenberg C, Navajas L, Vagenas DF, Bakker E, Vainzof M, Passos-Bueno MR, Takata RI, Van Ommen GJB, Zatz M, Den Dunnen JT. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization [Internet]. Neuromuscular Disorders. 1998 ; 8 417-452.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/s0960-8966(98)00050-9
Artigo de periodico
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families (1996)
Passos-Bueno, Maria Rita ; Moreira, E S; Marie, Suely Kazue Nagahashi; Bashir, R; Vasquez, L; Love, D R; Vainzof, Mariz ; Iughetti, P; Oliveira, J. R.; Bakker, E; Strachan, T
Source: Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families. Journal of Medical Genetics, v. 33, p. 97-102, 1996Tradução . . Disponível em: https://doi.org/10.1136/jmg.33.2.97. Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Moreira, E. S., Marie, S. K. N., Bashir, R., Vasquez, L., Love, D. R., et al. (1996). Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families. Journal of Medical Genetics, 33, 97-102. doi:10.1136/jmg.33.2.97
NLM
Passos-Bueno MR, Moreira ES, Marie SKN, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families [Internet]. Journal of Medical Genetics. 1996 ;33 97-102.[citado 2024 set. 19 ] Available from: https://doi.org/10.1136/jmg.33.2.97
Vancouver
Passos-Bueno MR, Moreira ES, Marie SKN, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families [Internet]. Journal of Medical Genetics. 1996 ;33 97-102.[citado 2024 set. 19 ] Available from: https://doi.org/10.1136/jmg.33.2.97
Artigo de periodico
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (lgmd2b) in three families allows refinement of the candidate region (1995)
Passos-Bueno, Maria Rita ; Bashir, R; Moreira, E S; Vainzof, Mariz ; Marie, Suely Kazue Nagahashi; Vasquez, L; Iughetti, P; Bakker, E; Keers, S; Stephenson, A; Strachan, T
Source: Genomics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (lgmd2b) in three families allows refinement of the candidate region. Genomics, v. 27, n. 1 , p. 192-5, 1995Tradução . . Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Bashir, R., Moreira, E. S., Vainzof, M., Marie, S. K. N., Vasquez, L., et al. (1995). Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (lgmd2b) in three families allows refinement of the candidate region. Genomics, 27( 1 ), 192-5.
NLM
Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SKN, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A, Strachan T. Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (lgmd2b) in three families allows refinement of the candidate region. Genomics. 1995 ;27( 1 ): 192-5.[citado 2024 set. 19 ]
Vancouver
Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SKN, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A, Strachan T. Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (lgmd2b) in three families allows refinement of the candidate region. Genomics. 1995 ;27( 1 ): 192-5.[citado 2024 set. 19 ]
Artigo de periodico
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers (1993)
Passos-Bueno, Maria Rita ; Wijmenga, C; Takata, R I; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Pavanello, R C M; Hewitt, J E; Bakker, E; Carvalho, A.; Akiyama, J; Frants, R R
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers. Human Molecular Genetics, v. 2 , n. 5 , p. 557-62, 1993Tradução . . Disponível em: https://doi.org/10.1093/hmg/2.5.557. Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Wijmenga, C., Takata, R. I., Marie, S. K. N., Vainzof, M., Pavanello, R. C. M., et al. (1993). No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers. Human Molecular Genetics, 2 ( 5 ), 557-62. doi:10.1093/hmg/2.5.557
NLM
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho A, Akiyama J, Frants RR. No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers [Internet]. Human Molecular Genetics. 1993 ;2 ( 5 ): 557-62.[citado 2024 set. 19 ] Available from: https://doi.org/10.1093/hmg/2.5.557
Vancouver
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho A, Akiyama J, Frants RR. No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers [Internet]. Human Molecular Genetics. 1993 ;2 ( 5 ): 557-62.[citado 2024 set. 19 ] Available from: https://doi.org/10.1093/hmg/2.5.557
Artigo de periodico
Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis (1993)
Passos-Bueno, Maria Rita ; Oliveira, J. R.; Bakker, E; Anderson, R D; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Roberds, S; Campbell, K P; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics, v. 2 , n. 11, p. 1945-7, 1993Tradução . . Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Oliveira, J. R., Bakker, E., Anderson, R. D., Marie, S. K. N., Vainzof, M., et al. (1993). Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics, 2 ( 11), 1945-7.
NLM
Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SKN, Vainzof M, Roberds S, Campbell KP, Zatz M. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics. 1993 ;2 ( 11): 1945-7.[citado 2024 set. 19 ]
Vancouver
Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SKN, Vainzof M, Roberds S, Campbell KP, Zatz M. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics. 1993 ;2 ( 11): 1945-7.[citado 2024 set. 19 ]
Artigo de periodico
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families (1993)
Passos-Bueno, Maria Rita ; Bakker, E; Marie, Suely Kazue Nagahashi; Pavanello, R C M; Vainzof, Mariz ; Carvalho, A. A.; Cohen, D; Beckmann, J S; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families. Human Molecular Genetics, v. 2 , n. 2 , p. 201-2, 1993Tradução . . Disponível em: https://doi.org/10.1093/hmg/2.2.201. Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Bakker, E., Marie, S. K. N., Pavanello, R. C. M., Vainzof, M., Carvalho, A. A., et al. (1993). Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families. Human Molecular Genetics, 2 ( 2 ), 201-2. doi:10.1093/hmg/2.2.201
NLM
Passos-Bueno MR, Bakker E, Marie SKN, Pavanello RCM, Vainzof M, Carvalho AA, Cohen D, Beckmann JS, Zatz M. Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families [Internet]. Human Molecular Genetics. 1993 ;2 ( 2 ): 201-2.[citado 2024 set. 19 ] Available from: https://doi.org/10.1093/hmg/2.2.201
Vancouver
Passos-Bueno MR, Bakker E, Marie SKN, Pavanello RCM, Vainzof M, Carvalho AA, Cohen D, Beckmann JS, Zatz M. Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families [Internet]. Human Molecular Genetics. 1993 ;2 ( 2 ): 201-2.[citado 2024 set. 19 ] Available from: https://doi.org/10.1093/hmg/2.2.201
Artigo de periodico
Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? (1993)
Passos-Bueno, Maria Rita ; Byth, B C; Rosemberg, Sérgio; Takata, R I; Bakker, E; Beggs, A H; Pavanello, R C M; Vainzof, Mariz ; Davies, K E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation?. American Journal of Medical Genetics, v. 46, n. 2 , p. 172-5, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Byth, B. C., Rosemberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? American Journal of Medical Genetics, 46( 2 ), 172-5. doi:10.1002/ajmg.1320460214
NLM
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 set. 19 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Vancouver
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 set. 19 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Artigo de periodico
Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk (1992)
Passos-Bueno, Maria Rita ; Bakker, E; Kneppers, A L J; Takata, R I; Rapaport, D; Dunnen, J T; Zatz, Mayana ; Ommen, G J B
Source: American Journal of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics, v. no 1992, n. 5 , p. 1150-5, 1992Tradução . . Acesso em: 19 set. 2024.
APA
Passos-Bueno, M. R., Bakker, E., Kneppers, A. L. J., Takata, R. I., Rapaport, D., Dunnen, J. T., et al. (1992). Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics, no 1992( 5 ), 1150-5.
NLM
Passos-Bueno MR, Bakker E, Kneppers ALJ, Takata RI, Rapaport D, Dunnen JT, Zatz M, Ommen GJB. Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics. 1992 ; no 1992( 5 ): 1150-5.[citado 2024 set. 19 ]
Vancouver
Passos-Bueno MR, Bakker E, Kneppers ALJ, Takata RI, Rapaport D, Dunnen JT, Zatz M, Ommen GJB. Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics. 1992 ; no 1992( 5 ): 1150-5.[citado 2024 set. 19 ]

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