Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature (2015)
- Authors:
- 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: 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 italo Barros 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: 28 dez. 2025. -
APA
Fontes, M. italo 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 M italo B, 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 2025 dez. 28 ] Available from: https://doi.org/10.1002/ajmg.a.37494 -
Vancouver
Fontes M italo B, 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 2025 dez. 28 ] 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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