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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.

    Fonte: Journal of Medical Genetics. Unidade: IB

    Assuntos: RETARDO MENTAL, DOENÇAS GENÉTICAS

    Acesso à fonteDOIComo citar
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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: 02 maio 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 maio 02 ] 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 maio 02 ] 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

    Fonte: Neuromuscular Disorders. Unidade: IB

    Assunto: GENÉTICA MÉDICA

    Acesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • 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: 02 maio 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 maio 02 ] 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 maio 02 ] Available from: https://doi.org/10.1016/s0960-8966(98)00050-9
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