Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature (2015)
- Authors:
- Fontes, Marshall I. B - Universidade Estadual de Campinas (UNICAMP)
- Santos, Ana P - Universidade Estadual de Campinas (UNICAMP)
- Molck, Miriam C - Universidade Estadual de Campinas (UNICAMP)
- Simioni, Milena - Universidade Estadual de Campinas (UNICAMP)
- Nascimento, Diogo L. L
- Andrade, Ana K. M - Universidade Federal de Alagoas (UFAL)
- Rosenberg, Carla
- Krepischi, Ana Cristina Victorino
- Appenzeller, Simone - Universidade Estadual de Campinas (UNICAMP)
- Monlleó, Isabela L - Universidade Federal de Alagoas (UFAL)
- Gil-da-Silva-Lopes, Vera Lúcia - Universidade Estadual de Campinas (UNICAMP)
- USP affiliated authors: ROSENBERG, CARLA - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB
- Unidade: IB
- DOI: 10.1002/ajmg.a.37494
- Subjects: CITOGENÉTICA; GENÓTIPOS; FENÓTIPOS; MALFORMAÇÕES; GENÉTICA MÉDICA; DELEÇÃO DE GENES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: online, p. 1-7, Dec. 2015
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
FONTES, Marshall I. B et al. Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature. American Journal of Medical Genetics Part A, p. 1-7, 2015Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.37494. Acesso em: 30 set. 2024. -
APA
Fontes, M. I. B., Santos, A. P., Molck, M. C., Simioni, M., Nascimento, D. L. L., Andrade, A. K. M., et al. (2015). Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature. American Journal of Medical Genetics Part A, 1-7. doi:10.1002/ajmg.a.37494 -
NLM
Fontes MIB, Santos AP, Molck MC, Simioni M, Nascimento DLL, Andrade AKM, Rosenberg C, Krepischi ACV, Appenzeller S, Monlleó IL, Gil-da-Silva-Lopes VL. Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature [Internet]. American Journal of Medical Genetics Part A. 2015 ; 1-7.[citado 2024 set. 30 ] Available from: https://doi.org/10.1002/ajmg.a.37494 -
Vancouver
Fontes MIB, Santos AP, Molck MC, Simioni M, Nascimento DLL, Andrade AKM, Rosenberg C, Krepischi ACV, Appenzeller S, Monlleó IL, Gil-da-Silva-Lopes VL. Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature [Internet]. American Journal of Medical Genetics Part A. 2015 ; 1-7.[citado 2024 set. 30 ] Available from: https://doi.org/10.1002/ajmg.a.37494 - Cytogenetically visible inversions are formed by multiple molecular mechanisms
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Informações sobre o DOI: 10.1002/ajmg.a.37494 (Fonte: oaDOI API)
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