Association of isolated hypogonadotropic hypogonadism, pronounced hypodontia and the Wolff-Parkinson-White syndrome
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2796.1994.tb00807.x/fullpdf
Reference15 articles.
1. The syndrome of anosmia with hypogonadotropic hypogonadism: a genetic study of 18 new families and a review;White;Am J Med Genet,1983
2. Syndrome of anosmia with hypogonadotropic hypogonadism (Kallmann syndrome);Lieblich;Am J Med,1982
3. Neurological findings in men with isolated hypogonadotropic hypogonadism;Schwankhaus;Neurology,1989
4. Xp22.3 deletions in isolated familial Kallmann's syndrome;Hardelin;J Clin Endocrinol Metab,1993
5. Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome;Schwanzel-Fukuda;Mol Brain Res,1989
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1. Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review;Dentistry Journal;2023-12-04
2. Olfactory Radioanatomical Findings in Patients With Cardiac Arrhythmias, COVID-19, and Healthy Controls;Cureus;2022-07-05
3. Association of olfactory neuropathy spectrum disorder and Wolff‐Parkinson‐White syndrome: A Report of a case;Clinical Case Reports;2020-05-25
4. Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations;International Journal of Paediatric Dentistry;2010-07
5. Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism;Proceedings of the National Academy of Sciences;2006-04-10
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