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Artigo de periodico
Macrosomia, obesity , macrocephaly and ocular abnormalities (momo syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome (1993)
Moretti-Ferreira, D; Koiffmann, Celia Priszkulnik ; Listik, M; Setian, Nuvarte; Wajntal, Anita
Source: American Journal Medical Genetics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORETTI-FERREIRA, D et al. Macrosomia, obesity , macrocephaly and ocular abnormalities (momo syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome. American Journal Medical Genetics, v. 46, n. ju 1993, p. 555-8, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460519. Acesso em: 04 nov. 2024.
APA
Moretti-Ferreira, D., Koiffmann, C. P., Listik, M., Setian, N., & Wajntal, A. (1993). Macrosomia, obesity , macrocephaly and ocular abnormalities (momo syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome. American Journal Medical Genetics, 46( ju 1993), 555-8. doi:10.1002/ajmg.1320460519
NLM
Moretti-Ferreira D, Koiffmann CP, Listik M, Setian N, Wajntal A. Macrosomia, obesity , macrocephaly and ocular abnormalities (momo syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome [Internet]. American Journal Medical Genetics. 1993 ;46( ju 1993): 555-8.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.1320460519
Vancouver
Moretti-Ferreira D, Koiffmann CP, Listik M, Setian N, Wajntal A. Macrosomia, obesity , macrocephaly and ocular abnormalities (momo syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome [Internet]. American Journal Medical Genetics. 1993 ;46( ju 1993): 555-8.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.1320460519
Artigo de periodico
Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth (1993)
Wajntal, Anita; Moretti-Ferreira, D; Souza, D. H.; Koiffmann, Celia Priszkulnik
Source: Dna and Cell Biology. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WAJNTAL, Anita et al. Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth. Dna and Cell Biology, v. 12, n. 3 , p. 227-31, 1993Tradução . . Acesso em: 04 nov. 2024.
APA
Wajntal, A., Moretti-Ferreira, D., Souza, D. H., & Koiffmann, C. P. (1993). Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth. Dna and Cell Biology, 12( 3 ), 227-31.
NLM
Wajntal A, Moretti-Ferreira D, Souza DH, Koiffmann CP. Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth. Dna and Cell Biology. 1993 ;12( 3 ): 227-31.[citado 2024 nov. 04 ]
Vancouver
Wajntal A, Moretti-Ferreira D, Souza DH, Koiffmann CP. Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth. Dna and Cell Biology. 1993 ;12( 3 ): 227-31.[citado 2024 nov. 04 ]
Trabalho de evento
Chromosome abnormalities and tumors in syndromes leading to overgrowth (1991)
Wajntal, Anita; Koiffmann, Celia Priszkulnik ; Souza, D. H.; Moretti-Ferreira, D
Source: Proceedings. Conference titles: Miami Bio-Technology Winter Symposium on Advances in Gene Technology: the Molecular Biology of Human Genetic Disease. Unidade: IB
Assunto: GENÉTICA ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WAJNTAL, Anita et al. Chromosome abnormalities and tumors in syndromes leading to overgrowth. 1991, Anais.. Miami: Short Reports, 1991. . Acesso em: 04 nov. 2024.
APA
Wajntal, A., Koiffmann, C. P., Souza, D. H., & Moretti-Ferreira, D. (1991). Chromosome abnormalities and tumors in syndromes leading to overgrowth. In Proceedings. Miami: Short Reports.
NLM
Wajntal A, Koiffmann CP, Souza DH, Moretti-Ferreira D. Chromosome abnormalities and tumors in syndromes leading to overgrowth. Proceedings. 1991 ;[citado 2024 nov. 04 ]
Vancouver
Wajntal A, Koiffmann CP, Souza DH, Moretti-Ferreira D. Chromosome abnormalities and tumors in syndromes leading to overgrowth. Proceedings. 1991 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo periodico
Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23 (1991)
Koiffmann, Celia Priszkulnik ; Gonzalez, Claudette Hajaj; Souza, D. H.; Odone Filho, Vicente; Kim, C A; Moretti-Ferreira, D; Wajntal, Anita
Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOIFFMANN, Celia Priszkulnik et al. Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 04 nov. 2024. , 1991
APA
Koiffmann, C. P., Gonzalez, C. H., Souza, D. H., Odone Filho, V., Kim, C. A., Moretti-Ferreira, D., & Wajntal, A. (1991). Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Koiffmann CP, Gonzalez CH, Souza DH, Odone Filho V, Kim CA, Moretti-Ferreira D, Wajntal A. Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 243.[citado 2024 nov. 04 ]
Vancouver
Koiffmann CP, Gonzalez CH, Souza DH, Odone Filho V, Kim CA, Moretti-Ferreira D, Wajntal A. Neuroblastoma in a child with dup 12q23 qter due to maternal translocation with breakpoints on 11q23 and 12q23. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 243.[citado 2024 nov. 04 ]
Trabalho de evento-resumo periodico
Estimation of penetrance of the sotos syndrome gene (1991)
Moretti-Ferreira, D; Wajntal, Anita; Otto, Paulo A
Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORETTI-FERREIRA, D e WAJNTAL, Anita e OTTO, Paulo A. Estimation of penetrance of the sotos syndrome gene. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 04 nov. 2024. , 1991
APA
Moretti-Ferreira, D., Wajntal, A., & Otto, P. A. (1991). Estimation of penetrance of the sotos syndrome gene. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Moretti-Ferreira D, Wajntal A, Otto PA. Estimation of penetrance of the sotos syndrome gene. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 152.[citado 2024 nov. 04 ]
Vancouver
Moretti-Ferreira D, Wajntal A, Otto PA. Estimation of penetrance of the sotos syndrome gene. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 152.[citado 2024 nov. 04 ]
Artigo de periodico
Macrocephaly , multiple lipomas , and hemangiomata (bannayan-zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? (1989)
Moretti-Ferreira, D; Koiffmann, Celia Priszkulnik ; Souza, D. H.; Diament, Aron Judka; Wajntal, Anita
Source: American Journal of Medical Genetics. Unidades: IB, FM
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORETTI-FERREIRA, D et al. Macrocephaly , multiple lipomas , and hemangiomata (bannayan-zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms?. American Journal of Medical Genetics, v. 34, n. 4 , p. 548-51, 1989Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320340419. Acesso em: 04 nov. 2024.
APA
Moretti-Ferreira, D., Koiffmann, C. P., Souza, D. H., Diament, A. J., & Wajntal, A. (1989). Macrocephaly , multiple lipomas , and hemangiomata (bannayan-zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? American Journal of Medical Genetics, 34( 4 ), 548-51. doi:10.1002/ajmg.1320340419
NLM
Moretti-Ferreira D, Koiffmann CP, Souza DH, Diament AJ, Wajntal A. Macrocephaly , multiple lipomas , and hemangiomata (bannayan-zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? [Internet]. American Journal of Medical Genetics. 1989 ;34( 4 ): 548-51.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.1320340419
Vancouver
Moretti-Ferreira D, Koiffmann CP, Souza DH, Diament AJ, Wajntal A. Macrocephaly , multiple lipomas , and hemangiomata (bannayan-zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? [Internet]. American Journal of Medical Genetics. 1989 ;34( 4 ): 548-51.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.1320340419

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