56 A RECOMBINATION EVENT CAUSING A DE NOVO DELETION OF THE STEROID 21-HYDROXYLASE GENE CYP21 [PDF]
Paul F. J. Koppens+6 more
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Precocious puberty in male with hypertension and hypokalemia; a definite diagnostic clue for 11β hydroxylase deficiency CAH. [PDF]
Pande M+3 more
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Hybridization of the complementary mRNAs for P450c21 (steroid 21-hydroxylase) and tenascin-X is prevented by sequence-specific binding of nuclear proteins. [PDF]
Mart Speek, Walter L. Miller
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Molecular genetics and epidemiology of steroid 21-hydroxylase deficiency. [PDF]
Koppens, PFJ
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Discovery and development of steroidal enzyme inhibitors as anti-cancer drugs: state-of-the-art and future perspectives. [PDF]
Cerra B, Gioiello A.
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Synergistic Effect of Partially Inactivating Mutations in Steroid 21-Hydroxylase Deficiency1 [PDF]
Andrej Nikoshkov+4 more
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Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency [PDF]
N. Weintrob+9 more
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Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical Implications. [PDF]
Concolino P, Falhammar H.
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Analysis of the Chimeric CYP21P/CYP21 Gene in Steroid 21-Hydroxylase Deficiency [PDF]
Hsien-Hsiung Lee+5 more
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