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Results:
1-15
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Results: 15
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
Authors:
Cervantes, A
Guevara-Yanez, R
Lopez, M
Monroy, N
Aguinaga, M
Valdez, H
Sierra, C
Canun, S
Guizar, J
Navarrete, C
Zafra, G
Salamanca, F
Kofman-Alfaro, S
Citation: A. Cervantes et al., PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype, CLIN GENET, 60(5), 2001, pp. 385-392
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
Authors:
Valdes-Flores, M
Vaca, AJ
Kofman-Alfaro, S
Cuevas-Covarrubias, S
Citation: M. Valdes-flores et al., Characterization of a novel point mutation (Arg432His) in X-linked ichthyosis, ACT DER-VEN, 81(1), 2001, pp. 54-55
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
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
Authors:
Canto, P
de la Chesnaye, E
Lopez, M
Cervantes, A
Chavez, B
Vilchis, F
Reyes, E
Ulloa-Aguirre, A
Kofman-Alfaro, S
Mendez, JP
Citation: P. Canto et al., A mutation in the 5 ' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism, J CLIN END, 85(5), 2000, pp. 1908-1911
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
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
Authors:
Mendez, JP
Canto, P
Lopez, M
de la Chesnaye, E
Torres, L
Chavez, B
Ulloa-Aguirre, A
Kofman-Alfaro, S
Citation: Jp. Mendez et al., Scant XYqh- testicular cells with normal SRY was enough to differentiate bilateral testes in a 45,X/46,XYqh- patient, EUR J OB GY, 87(2), 1999, pp. 159-162
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
Authors:
Graves, PE
Davis, D
Erickson, RP
Lopez, M
Kofman-Alfaro, S
Mendez, JP
Speer, IE
Citation: Pe. Graves et al., Ascertainment and mutational studies of SRY in nine XY females, AM J MED G, 83(2), 1999, pp. 138-139
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
Authors:
Rivera, MR
Avila, CA
Kofman-Alfaro, S
Citation: Mr. Rivera et al., Distal arthrogryposis type IIB: probable autosomal recessive inheritance, CLIN GENET, 56(1), 1999, pp. 95-97
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