Author

F. Kutten

Observed names: F Kutten, Frédéarique Kuttenn

Institution: Hôpital Necker-Enfants Malades

Observed institution: Hôpital Necker-Enfants Malades

OpenAlex ID: A5072037282

Impaired Sexual and Reproductive Outcomes in Women with Classical Forms of Congenital Adrenal Hyperplasia

2007 · F. Gastaud, C. Bouvattier, et al. · The Journal of Clinical Endocrinology & Metabolism · 188

Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency

1995 · Benoit Barbat, Any Bogyo, et al. · Human Mutation · 69

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

1986 · E. Mornet, P. Couillin, et al. · Human Genetics · 29

[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].

1992 · E Mornet, J Boué, et al. · PubMed

Works count: 4

Citation count: 286

H-index: 3

I10-index: 3