A unique haplotype of CCX copy number variation from the clinics of congenital adrenal hyperplasia to evolutionary genetics
Target ArticleEdit
A unique haplotype of CCX copy number variation from the clinics of congenital adrenal hyperplasia to evolutionary genetics; M Doleschall, A Luczay, K Koncz, K Hadzsievae; 2017; 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.