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Results: 1-3 |
Results: 3
Refined localization of twenty-one genes in subregion p13.1 of human chromosome 1
Authors: Chelala, C Imbeaud, S Devignes, MD Zoorob, R Auffray, C
Citation: C. Chelala et al., Refined localization of twenty-one genes in subregion p13.1 of human chromosome 1, CYTOG C GEN, 92(3-4), 2001, pp. 209-212
Autosomal recessive segregation of a truncating mutation of anti-mulleriantype II receptor in a family affected by the persistent mullerian duct syndrome contrasts with its dominant negative activity in vitro
Authors: Messika-Zeitoun, L Gouedard, L Belville, C Dutertre, M Lins, L Imbeaud, S Hughes, IA Picard, JY Josso, N di Clemente, N
Citation: L. Messika-zeitoun et al., Autosomal recessive segregation of a truncating mutation of anti-mulleriantype II receptor in a family affected by the persistent mullerian duct syndrome contrasts with its dominant negative activity in vitro, J CLIN END, 86(9), 2001, pp. 4390-4397
Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with anovel mutation in the DAX-1 gene
Authors: Caron, P Imbeaud, S Bennet, A Plantavid, M Camerino, G Rochiccioli, P
Citation: P. Caron et al., Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with anovel mutation in the DAX-1 gene, J CLIN END, 84(10), 1999, pp. 3563-3569
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