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Biometrics, ISSN 0006-341X, 09/2017, Volume 73, Issue 3, pp. 1054 - 1055
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2017, Volume 127, Issue 3, p. 796
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2017, Volume 127, Issue 3, pp. 796 - 797
Journal Article
Endocrine Reviews, ISSN 0163-769X, 02/2016, Volume 2016, Issue 1, pp. 4 - 22
The neuroendocrine regulation of reproduction is an intricate process requiring the exquisite coordination of an assortment of cellular networks, all... 
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 1945-7197, 02/2017, Volume 102, Issue 2, p. 337
Journal Article
1987, Wiley medical publication., ISBN 0471849928, xxv, 518
Book
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 03/2019, Volume 104, Issue 8, pp. 3403 - 3414
A subset of men following completion of puberty subsequently experience functional hypogonadotropic hypogonadism (FHH) secondary to excessive exercise and/or... 
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2005, Volume 102, Issue 6, pp. 2129 - 2134
Journal Article
Journal Article
Endocrine Reviews, ISSN 0163-769X, 12/2015, Volume 36, Issue 6, pp. 603 - 621
The neuroendocrine regulation of reproduction is an intricate process requiring the exquisite coordination of an assortment of cellular networks, all... 
Reviews
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2010, Volume 107, Issue 34, pp. 15140 - 15144
Between the genetic extremes of rare monogenic and common polygenic diseases lie diverse oligogenic disorders involving mutations in more than one locus in... 
Deficiency diseases | Sex hormones | Nervous system diseases | Disease models | Medical genetics | Genetic diseases | Genetic mutation | Kallmann syndrome | Human genetics | Hypogonadism | Rare variant | Digenic | Idiopathic hypogonadotropic hypogonadism | FGFR1 | idiopathic hypogonadotropic hypogonadism | GPR54 | MULTIDISCIPLINARY SCIENCES | CLINICAL HETEROGENEITY | MISSENSE MUTATIONS | PUBERTY | digenic | GENE | BARDET-BIEDL-SYNDROME | LINKED KALLMANN-SYNDROME | FIBROBLAST-GROWTH-FACTOR-RECEPTOR-1 | GNRH RECEPTOR | rare variant | Receptors, LHRH - genetics | Humans | Male | Gene Regulatory Networks | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Case-Control Studies | Receptors, Peptide - genetics | Genetic Variation | DNA Mutational Analysis | Female | Neuropeptides - genetics | Fibroblast Growth Factor 8 - genetics | Kallmann Syndrome - genetics | Extracellular Matrix Proteins - genetics | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Hypogonadism - genetics | Homozygote | Phenotype | Pedigree | Gastrointestinal Hormones - genetics | Heterozygote | Models, Genetic | Receptors, G-Protein-Coupled - genetics | Mutation | Receptors, Kisspeptin-1 | Gonadotropin-Releasing Hormone - deficiency | Cohort Studies | Multifactorial diseases | Genetic aspects | Hormones | Gonadotropin | Health aspects | Pathogens | Genetics | Genetic disorders | Pathogenesis | Index Medicus | Biological Sciences
Journal Article
ENDOCRINE REVIEWS, ISSN 0163-769X, 02/2017, Volume 38, Issue 1, pp. 1 - 2
Journal Article
ENDOCRINOLOGY, ISSN 0013-7227, 02/2017, Volume 158, Issue 2, pp. 197 - 198
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2007, Volume 357, Issue 9, pp. 863 - 873
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2013, Volume 92, Issue 5, pp. 725 - 743
Journal Article