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A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor.
INSERM Unité 135, Institut Fédératif de Recherche 21, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France.
PMID: 9371856 [PubMed - indexed for MEDLINE]
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Cited by 10 PubMed Central articles
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Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Kim HG, Kurth I, Lan F, Meliciani I, Wenzel W, Eom SH, Kang GB, Rosenberger G, Tekin M, Ozata M, et al.
Am J Hum Genet. 2008 Oct; 83(4):511-9. Epub 2008 Oct 2.
[Am J Hum Genet. 2008]
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Association of the timing of puberty with a chromosome 2 locus.
Wehkalampi K, Widén E, Laine T, Palotie A, Dunkel L.
J Clin Endocrinol Metab. 2008 Dec; 93(12):4833-9. Epub 2008 Sep 23.
[J Clin Endocrinol Metab. 2008]
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Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
Falardeau J, Chung WC, Beenken A, Raivio T, Plummer L, Sidis Y, Jacobson-Dickman EE, Eliseenkova AV, Ma J, Dwyer A, et al.
J Clin Invest. 2008 Aug; 118(8):2822-31.
[J Clin Invest. 2008]
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