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Trabalho de evento-resumo periodico
Familial cases of xx males: argument for a common origin of y negative 46 xx male and true hermaphrodites (1989)
Abbas, N.; Boucekkine, C.; Moreira-Filho, Carlos Alberto; Ternes-Pereira, E.; Cabral de Almeida, J. C.; Fellous, Marc
Source: Cytogenetics and Cell Genetics. Conference titles: International Workshop on Human Gene Mapping. Unidade: ICB
Subjects: GENETICA (CONGRESSOS;CONFERÊNCIAS), HERMAFRODITISMO, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABBAS, N. et al. Familial cases of xx males: argument for a common origin of y negative 46 xx male and true hermaphrodites. Cytogenetics and Cell Genetics. Basel: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 01 jun. 2024. , 1989
APA
Abbas, N., Boucekkine, C., Moreira-Filho, C. A., Ternes-Pereira, E., Cabral de Almeida, J. C., & Fellous, M. (1989). Familial cases of xx males: argument for a common origin of y negative 46 xx male and true hermaphrodites. Cytogenetics and Cell Genetics. Basel: Instituto de Ciências Biomédicas, Universidade de São Paulo.
NLM
Abbas N, Boucekkine C, Moreira-Filho CA, Ternes-Pereira E, Cabral de Almeida JC, Fellous M. Familial cases of xx males: argument for a common origin of y negative 46 xx male and true hermaphrodites. Cytogenetics and Cell Genetics. 1989 ; 51 948.[citado 2024 jun. 01 ]
Vancouver
Abbas N, Boucekkine C, Moreira-Filho CA, Ternes-Pereira E, Cabral de Almeida JC, Fellous M. Familial cases of xx males: argument for a common origin of y negative 46 xx male and true hermaphrodites. Cytogenetics and Cell Genetics. 1989 ; 51 948.[citado 2024 jun. 01 ]
Trabalho de evento-resumo periodico
Dominant hereditary sphenocytosis (hs) is linked to the gene for the erytrocyte membrane protein ankyrin (1989)
Forget, B G; Lux, S E; Agre, P; Watkins, P C; Costa, F F
Source: Cytogenetics and Cell Genetics. Conference titles: International Workshop on Human Gene Mapping. Unidade: FMRP
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FORGET, B G et al. Dominant hereditary sphenocytosis (hs) is linked to the gene for the erytrocyte membrane protein ankyrin. Cytogenetics and Cell Genetics. [S.l.]: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 01 jun. 2024. , 1989
APA
Forget, B. G., Lux, S. E., Agre, P., Watkins, P. C., & Costa, F. F. (1989). Dominant hereditary sphenocytosis (hs) is linked to the gene for the erytrocyte membrane protein ankyrin. Cytogenetics and Cell Genetics. Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Forget BG, Lux SE, Agre P, Watkins PC, Costa FF. Dominant hereditary sphenocytosis (hs) is linked to the gene for the erytrocyte membrane protein ankyrin. Cytogenetics and Cell Genetics. 1989 ;51( 1 ): 999.[citado 2024 jun. 01 ]
Vancouver
Forget BG, Lux SE, Agre P, Watkins PC, Costa FF. Dominant hereditary sphenocytosis (hs) is linked to the gene for the erytrocyte membrane protein ankyrin. Cytogenetics and Cell Genetics. 1989 ;51( 1 ): 999.[citado 2024 jun. 01 ]

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