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Results: 1-9 |
Results: 9
Clinical expression and SRY gene analysis in XY subjects lacking gonadal tissue
Authors: Zenteno, JC Jimenez, AL Canto, P Valdez, H Mendez, JP Kofman-Alfaro, S
Citation: Jc. Zenteno et al., Clinical expression and SRY gene analysis in XY subjects lacking gonadal tissue, AM J MED G, 99(3), 2001, pp. 244-247
Novel molecular defects in the androgen receptor gene of Mexican patients with androgen insensitivity
Authors: Chavez, B Vilchis, F Zenteno, JC Larrea, F Kofman-Alfaro, S
Citation: B. Chavez et al., Novel molecular defects in the androgen receptor gene of Mexican patients with androgen insensitivity, CLIN GENET, 59(3), 2001, pp. 185-188
Kallmann syndrome (hypogonadotropism-anosmia) and Klippel-Feil anomaly in the same patient
Authors: Zenteno, JC Venegas, C Santiago, E Kofman-Alfaro, S
Citation: Jc. Zenteno et al., Kallmann syndrome (hypogonadotropism-anosmia) and Klippel-Feil anomaly in the same patient, CLIN DYSMOR, 9(1), 2000, pp. 69-70
Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA
Authors: Jimenez, AL Kofman-Alfaro, S Berumen, J Hernandez, E Canto, P Mendez, JP Zenteno, JC
Citation: Al. Jimenez et al., Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA, AM J MED G, 93(5), 2000, pp. 417-420
Additional evidence of a continuous phenotypic spectrum in the short rib-polydactyly syndromes
Authors: Blanco, ME Valdes, JM Kofman-Alfaro, S Zenteno, JC
Citation: Me. Blanco et al., Additional evidence of a continuous phenotypic spectrum in the short rib-polydactyly syndromes, PEDIAT PATH, 18(2), 1999, pp. 143-150
Renal abnormalities in patients with Kallmann syndrome
Authors: Zenteno, JC Mendez, JP Maya-Nunez, G Ulloa-Aguirre, A Kofman-Alfaro, S
Citation: Jc. Zenteno et al., Renal abnormalities in patients with Kallmann syndrome, BJU INT, 83(4), 1999, pp. 383-386
Evidence that AEC syndrome and Bowen-Armstrong syndrome are variable expressions of the same disease
Authors: Zenteno, JC Venegas, C Kofman-Alfaro, S
Citation: Jc. Zenteno et al., Evidence that AEC syndrome and Bowen-Armstrong syndrome are variable expressions of the same disease, PEDIAT DERM, 16(2), 1999, pp. 103-107
An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis
Authors: Maya-Nunez, G Torres, L Ulloa-Aguirre, A Zenteno, JC Cuevas-Covarrubias, S Saavedra-Ontiveros, D Kofman-Alfaro, S Mendez, JP
Citation: G. Maya-nunez et al., An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis, CLIN ENDOCR, 50(2), 1999, pp. 157-162
Evidence for genetic heterogeneity in male pseudohermaphroditism due to leydig cell hypoplasia
Authors: Zenteno, JC Canto, P Kofman-Alfaro, S Mendez, JP
Citation: Jc. Zenteno et al., Evidence for genetic heterogeneity in male pseudohermaphroditism due to leydig cell hypoplasia, J CLIN END, 84(10), 1999, pp. 3803-3806
Risultati: 1-9 |