Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins (2017)
Jehee, Fernanda S; Oliveira, Valdirene T. de; Gurgel Giannetti, Juliana; Pietra, Rafaella X; Rubatino, Fernando V. M; Carobin, Natália V; Vianna, Gabrielle S; Freitas, Mariana L. de; Fernandes, Karla S; Ribeiro, Beatriz S. V; Brüggenwirth, Hennie T; Ali-Amin, Roza; White, Janson J; Akdemir, Zeynep C; Jhangiani, Shalini N; Gibbs, Richard A; Lupski, James R; Varela, Monica C; Koiffmann, Celia Priszkulnik 
; Rosenberg, Carla ; Carvalho, Cláudia M. B
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, GENÉTICA MÉDICA, DELEÇÃO DE GENES, FENÓTIPOS, OBESIDADE, RETARDO MENTAL
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JEHEE, Fernanda S et al. Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins. American Journal of Medical Genetics. Part A, p. 1-5, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.38315. Acesso em: 03 nov. 2024.APA
Jehee, F. S., Oliveira, V. T. de, Gurgel Giannetti, J., Pietra, R. X., Rubatino, F. V. M., Carobin, N. V., et al. (2017). Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins. American Journal of Medical Genetics. Part A, 1-5. doi:10.1002/ajmg.a.38315NLM
Jehee FS, Oliveira VT de, Gurgel Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, Freitas ML de, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R, White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann CP, Rosenberg C, Carvalho CMB. Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 1-5.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.38315Vancouver
Jehee FS, Oliveira VT de, Gurgel Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, Freitas ML de, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R, White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann CP, Rosenberg C, Carvalho CMB. Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 1-5.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.38315
