AAAAAA
Results:
1-7
|
Results: 7
Authors:
Ottolenghi, C
Moreira, C
Mendonca, BB
Barbieri, M
Fellous, M
Berkovitz, GD
McElreavey, K
Citation: C. Ottolenghi et al., Absence of mutations involving the lim homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis, J CLIN END, 86(6), 2001, pp. 2465-2469
Authors:
Perera, EM
Martin, H
Seeherunvong, T
Kos, L
Hughes, IA
Hawkins, JR
Berkovitz, GD
Citation: Em. Perera et al., Tescalcin, a novel gene encoding a putative EF-hand Ca2+-binding protein, Col9a3, and renin are expressed in the mouse testis during the early stagesof gonadal differentiation, ENDOCRINOL, 142(1), 2001, pp. 455-463
Authors:
Lim, HN
Berkovitz, GD
Hughes, IA
Hawkins, JR
Citation: Hn. Lim et al., Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination, HUM GENET, 107(6), 2000, pp. 650-652
Authors:
Wisniewski, AB
Migeon, CJ
Meyer-Bahlburg, HFL
Gearhart, JP
Berkovitz, GD
Brown, TR
Money, J
Citation: Ab. Wisniewski et al., Complete androgen insensitivity syndrome: Long-term medical, surgical, andpsychosexual outcome, J CLIN END, 85(8), 2000, pp. 2664-2669
Authors:
Bick, DP
McCorkle, D
Stanley, WS
Stern, HJ
Staszak, P
Berkovitz, GD
Meyers, CM
Kelley, RI
Citation: Dp. Bick et al., Prenatal diagnosis of Smith-Lemli-Opitz syndrome in a pregnancy with low maternal serum oestriol and a sex-reversed fetus, PRENAT DIAG, 19(1), 1999, pp. 68-71
Authors:
Berkovitz, GD
Seeherunvong, T
Citation: Gd. Berkovitz et T. Seeherunvong, Molecular basis of disorders of sexual differentiation, CONT ENDOC, 10, 1999, pp. 1-9
Authors:
Fuqua, JS
Berkovitz, GD
Citation: Js. Fuqua et Gd. Berkovitz, Growth hormone excess in a child with neurofibromatosis type 1 and optic pathway tumor: A patient report, CLIN PEDIAT, 37(12), 1998, pp. 749-752
Risultati:
1-7
|