Congenital heart disease associated with sporadic Kallmann syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference15 articles.
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1. WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome;EMBO reports;2017-12-20
2. WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome;2017-10-10
3. Congenital Hypogonadotropic Hypogonadism in Males: Clinical Features and Pathophysiology;Male Hypogonadism;2017
4. Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development;Sexual Development;2016-04-08
5. Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience;Annals of Pediatric Endocrinology & Metabolism;2015
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