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Biblio

3 resultats trouvés

Filtres: Auteur is Naud-Saudreau, Catherine [Clear All Filters]

C

Geoffron S, Habib WAbi, Chantot-Bastaraud S, Dubern B, Steunou V, Azzi S, Afenjar A, Busa T, Canton APinheiro, Chalouhi C et al.. 2018. Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 103:2436-2446.

Cohen E, Pham A, Dastot F, Collot N, Afenjar A, Carel J-C, Furioli J, Leger J, Leheup B, Mignot B et al.. 2016. Contribution of GLI2 Mutations to Pituitary Deficits and Delineation of the Associated Phenotypic Spectrum. HORMONE RESEARCH IN PAEDIATRICS. 86:34-35.

I

Giabicani E, Willems M, Steunou V, Chantot-Bastaraud S, Thibaud N, Habib WAbi, Azzi S, Lam B, Berard L, Bony-Trifunovic H et al.. 2020. Increasing knowledge in IGF1R defects: lessons from 35 new patients. JOURNAL OF MEDICAL GENETICS. 57:160-168.