A are Duplicated 21-Hydroxylase Haplotype and a de Novo Mutation A Family Analysis
Revision as of 22:48, 11 August 2022 by 187.21.138.9 (talk) (Created page with "== Target Article == A are Duplicated 21-Hydroxylase Haplotype and a de Novo Mutation A Family Analysis; SM Baumgartner; 2003; doi_citing_unknown == Retraction == Bilateral ovarian steroid cell tumor in congenital adrenal hyperplasia due to classic 11ß-hydroxylase deficiency ; Firdevs Bas Nucin Saka Feyza Darendeliler Siki Tuzlah Ridvan Ilhan Ruveyde Bundak Hulya Gonuz; 06/01/2000 ; https://doi.org/0.1515/JPEM.2000.13.6.663 == Citation piece == Note: Open to app...")
Target ArticleEdit
A are Duplicated 21-Hydroxylase Haplotype and a de Novo Mutation A Family Analysis; SM Baumgartner; 2003; doi_citing_unknown
RetractionEdit
Bilateral ovarian steroid cell tumor in congenital adrenal hyperplasia due to classic 11ß-hydroxylase deficiency ; Firdevs Bas Nucin Saka Feyza Darendeliler Siki Tuzlah Ridvan Ilhan Ruveyde Bundak Hulya Gonuz; 06/01/2000
Citation pieceEdit
Note: Open to append information.