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1 Ergebnisse
1
Heterozygosis for CYP21A2 mutation considered as 21-hydroxy..:
Soardi, Fernanda Caroline
;
Lemos-Marini, Sofia Helena Valente de
;
Coeli, Fernanda Borchers
...
Arquivos Brasileiros de Endocrinologia & Metabologia. , 2008
Link:
https://repositorio.unifesp.br/handle/11600/4626
RT Journal T1
Heterozygosis for CYP21A2 mutation considered as 21-hydroxylase deficiency in neonatal screening ; Heterozigose para mutação no gene CYP21A2 considerada como deficiência de 21-hidroxilase na triagem neonatal
UL https://suche.suub.uni-bremen.de/peid=base-ftunivfsaopaulo:oai:repositorio.unifesp.br:11600_4626&Exemplar=1&LAN=DE A1 Soardi, Fernanda Caroline A1 Lemos-Marini, Sofia Helena Valente de A1 Coeli, Fernanda Borchers A1 Maturana, Víctor Gonçalves A1 Silva, Márcia Duarte Barbosa da A1 Bernardi, Renan Darin A1 Justo, Giselle Zenker UNIFESP A1 Mello, Maricilda Palandi de PB Sociedade Brasileira de Endocrinologia e Metabologia YR 2008 K1 Neonatal screening K1 Minigenes K1 21-hydroxylase deficiency K1 CYP21A2 mutations K1 Triagem neonatal K1 Mutações CYP21A2 K1 Deficiência de 21-hidroxilase JF Arquivos Brasileiros de Endocrinologia & Metabologia LK http://dx.doi.org/https://repositorio.unifesp.br/handle/11600/4626 DO https://repositorio.unifesp.br/handle/11600/4626 SF ELIB - SuUB Bremen
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