Authors:
Witchel, SF
White, C
Seigel, ME
Aston, CE
Citation: Sf. Witchel et al., Inconsistent effects of the proline(12) -> alanine variant of the peroxisome proliferator-activated receptor-gamma 2 gene on body mass index in children and adolescent girls, FERT STERIL, 76(4), 2001, pp. 741-747
Authors:
Tomboc, M
Lee, PA
Mitwally, MF
Schneck, FX
Bellinger, M
Witchel, SF
Citation: M. Tomboc et al., Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism, J CLIN END, 85(11), 2000, pp. 4013-4018
Authors:
Kahsar-Miller, M
Azziz, R
Feingold, E
Witchel, SF
Citation: M. Kahsar-miller et al., A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome, FERT STERIL, 74(6), 2000, pp. 1237-1240
Authors:
Witchel, SF
Fagerli, J
Siegel, J
Smith, R
Mitwally, MF
Lewy, V
Arslanian, S
Lee, PA
Citation: Sf. Witchel et al., No association between body mass index and beta(3)-adrenergic receptor variant (W64R) in children with premature pubarche and adolescent girls with hyperandrogenism, FERT STERIL, 73(3), 2000, pp. 509-515
Authors:
Moran, C
Azziz, R
Carmina, E
Dewailly, D
Fruzzetti, F
Ibanez, L
Knochenhauer, ES
Marcondes, JAM
Mendonca, BB
Pignatelli, D
Pugeat, M
Rohmer, V
Speiser, PW
Witchel, SF
Citation: C. Moran et al., 21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study, AM J OBST G, 183(6), 2000, pp. 1468-1474
Citation: Sf. Witchel et Rr. Smith, Glucocorticoid resistance in premature pubarche and adolescent hyperandrogenism, MOL GEN MET, 66(2), 1999, pp. 137-141
Citation: Sf. Witchel et al., Leptin concentrations in precocious puberty or untimely puberty with and without GnRH analogue therapy, J PED END M, 12(6), 1999, pp. 839-845
Citation: Sf. Witchel et S. Arslanian, Ovarian responses to hCG stimulation: insulin resistance/hyperinsulinaemiavs. insulin deficiency, CLIN ENDOCR, 51(1), 1999, pp. 127-130
Authors:
Escobar-Morreale, HF
San Millan, JL
Smith, RR
Sancho, J
Witchel, SF
Citation: Hf. Escobar-morreale et al., The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations, FERT STERIL, 72(4), 1999, pp. 629-638
Authors:
Fagerli, J
Schneck, FX
Lee, PA
Bellinger, MF
Witchel, SF
Citation: J. Fagerli et al., Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia, FERT STERIL, 71(4), 1999, pp. 697-700