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2010, Frontiers of hormone research, ISBN 3805586175, Volume 39., x, 174
Over the past decade, the understanding of the processes involved in the regulation of gonadotropin-releasing hormone and its dysfunction has greatly... 
Kallmann Syndrome | Hypogonadism | genetics
Book
Case Report - MRI findings in Kallmann syndrome, 10/2004
Kallmann syndrome (KS) is a neuronal migration disorder characterised by hypogonadotrophic hypogonadism and anosmia or hyposmia. Five patients with clinical... 
Neurology | Kallmann syndrome, Hypogonadotrophic hypogonadism, Anosmia, Magnetic Resonance Imaging, Olfactory system. ni04168
Journal
2010, Frontiers of hormone research, ISBN 9783805586177, Volume 39
Web Resource
Brain, ISSN 0006-8950, 2013, Volume 136, Issue 2, pp. 522 - 535
Journal Article
Journal Article
Medicine (United States), ISSN 0025-7974, 07/2018, Volume 97, Issue 27
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Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2015, Volume 125, Issue 6, pp. 2413 - 2428
Journal Article
Medicine (United States), ISSN 0025-7974, 09/2017, Volume 96, Issue 35, pp. e7974 - e7974
Journal Article
EMBO reports, ISSN 1469-221X, 02/2018, Volume 19, Issue 2, pp. 269 - 289
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 12/2017, Volume 8, pp. 210 - 210
We report a Japanese female patient presenting with classic features of CHARGE syndrome, including choanal atresia, growth and development retardation, ear... 
CHARGE syndrome | KMT2D | Kabuki syndrome | Phenotypic overlap | CHD7 | MLL2 | CHD7 MUTATION | ANOMALIES | PHENOTYPIC SPECTRUM | DEFICIENCY | COLOBOMA | CHOANAL ATRESIA | phenotypic overlap | GENETICS & HEREDITY | OVERLAP | KALLMANN-SYNDROME | PATIENT | Genetic research | Health aspects | Genetic aspects
Journal Article