Mutations in human gonadotropin genes and their physiologic significance in puberty and reproduction von Layman, Lawrence C

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Editorial: BMP15—The First True Ovarian Determinant Gene on the X-Chromosome? von Layman, Lawrence C

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Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism von Bhagavath, Balasubramanian, Podolsky, Robert H., Ozata, Metin, Bolu, Erol, Bick, David P., Kulharya, Anita, Sherins, Richard J., Layman, Lawrence C.

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Human gene mutations causing infertility von Layman, L C

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The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism von Bhagavath, Balasubramanian, Ozata, Metin, Ozdemir, I.C., Bolu, Erol, Bick, David P., Sherins, Richard J., Layman, Lawrence C.

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Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism von Layman, Lawrence C, Cohen, David P, Jin, Mei, Xie, Jun, Li, Zhu, Reindollar, Richard H, Bolbolan, Shahla, Bick, David P, Sherins, Richard R, Duck, L. Wayne, Musgrove, Lois C, Sellers, Jeffrey C, Neill, Jimmy D

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Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone β-Subunit Gene von Layman, Lawrence C, Lee, Eun-Jig, Peak, Douglas B, Namnoum, Anne B, Vu, Kenneth V, van Lingen, Barbara L, Gray, Mark R, McDonough, Paul G, Reindollar, Richard H, Jameson, J. Larry

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Mutations of follicle stimulating hormone-β and its receptor in human and mouse: genotype/phenotype von Layman, Lawrence C, McDonough, Paul G

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Autoantibodies against the FSH receptor: association or causation? von Layman, Lawrence C.

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The finnish follicle-stimulating hormone receptor gene mutation is rare in North american women with 46,xx ovarian failure von Layman, Lawrence C, Amde, Sewit, Cohen, David P, Jin, Mei, Xie, Jun

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The role of LH and FSH in ovarian androgen secretion and ovarian follicular development: Clinical studies in a patient with isolated FSH deficiency and multicystic ovaries von BARNES, Randall B, NAMNOUM, Anne B, ROSENFIELD, Robert L, LAYMA, Lawrence C

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Mutations in the Follicle-Stimulating Hormone-Beta (FSHβ) and FSH Receptor Genes in Mice and Humans von Layman, Lawrence C.

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Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay von ACHERMANN, J. C, GU, W.-X, CROWLEY, W. F, LAYMAN, L. C, JAMESON, J. L, KOTLAR, T. J, MEEKS, J. J, SABACAN, L. P, SEMINARA, S. B, HABIBY, R. L, HINDMARSH, P. C, BICK, D. P, SHERINS, R. J

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Clinical phenotype and infertility treatment in a male with hypogonadotropic hypogonadism due to mutations Ala129Asp/Arg262Gln of the gonadotropin-releasing hormone receptor von Layman, Lawrence C, Cohen, David P, Xie, Jun, Smith, Gary D

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The Molecular Basis of Human Hypogonadotropic Hypogonadism von Layman, Lawrence C.

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Analysis of the Cys82Arg mutation in follicle-stimulating hormone beta (FSHβ) using a novel FSH expression vector von Clark, Andrew D, Layman, Lawrence C

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Familial gonadotropin-releasing hormone resistance and hypogonadotropic hypogonadism in a family with multiple affected individuals von Layman, Lawrence C, McDonough, Paul G, Cohen, David P, Maddox, Mary, Tho, Sandra P.T, Reindollar, Richard H

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Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarrays von Xu, Ning, Podolsky, Robert H., Chudgar, Pranav, Chorich, Lynn P., Liu, Chunmei, McDonough, Paul G., Warrington, Janet A., Layman, Lawrence C.

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Effect of Follicle-Stimulating Hormone on Ovarian Androgen Production in a Woman with Isolated Follicle-Stimulating Hormone Deficiency von Namnoum, Anne, Barnes, Randall B, Layman, Lawrence C, Rosenfield, Robert L

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Administration of progesterone before oocyte retrieval negatively affects the implantation rate von Sohn, Sae H, Penzias, Alan S, Emmi, Adelina M, Dubey, Anil K, Layman, Lawrence C, Reindollar, Richard H, DeCherney, Alan H

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