Fraxf in a patient with chromosome 8 duplication (1996)
- Authors:
- USP affiliated authors: MORGANTE, ANGELA MARIA VIANNA - IB ; OTTO, PAULO ALBERTO - IB ; ROSENBERG, CARLA - IB ; MINGRONI NETTO, REGINA CELIA - IB
- Unidade: IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.33, n.7 , p.611-4, 1996
-
ABNT
VIANNA-MORGANTE, Angela M et al. Fraxf in a patient with chromosome 8 duplication. Journal of Medical Genetics, v. 33, n. 7 , p. 611-4, 1996Tradução . . Acesso em: 09 nov. 2024. -
APA
Vianna-Morgante, A. M., Mingroni Netto, R. C., Barbosa, A. C. C., Otto, P. A., & Rosenberg, C. (1996). Fraxf in a patient with chromosome 8 duplication. Journal of Medical Genetics, 33( 7 ), 611-4. -
NLM
Vianna-Morgante AM, Mingroni Netto RC, Barbosa ACC, Otto PA, Rosenberg C. Fraxf in a patient with chromosome 8 duplication. Journal of Medical Genetics. 1996 ;33( 7 ): 611-4.[citado 2024 nov. 09 ] -
Vancouver
Vianna-Morgante AM, Mingroni Netto RC, Barbosa ACC, Otto PA, Rosenberg C. Fraxf in a patient with chromosome 8 duplication. Journal of Medical Genetics. 1996 ;33( 7 ): 611-4.[citado 2024 nov. 09 ] - Chromosome imbalances in syndromic hearing loss
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