Author:
Quinton Richard,Duke Véronique M.,Robertson Alexis,Kirk Jeremy M. W.,Matfin Glenn,De Zoysa Priyal A.,Azcona Christina,MacColl Gavin S.,Jacobs Howard S.,Conway Gerard S.,Besser Michael,Stanhope Richard G.,Bouloux Pierre-Marc G.
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Reference69 articles.
1. Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay;Achermann;Journal of Clinical Endocrinology and Metabolism,1999
2. Intragenic deletion of the KALIG-I gene in Kallmann’s syndrome;Bick;New England Journal of Medicine,1992
3. A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3);Bouloux;Nucleic Acids Research,1991
4. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus;Bouloux;Clinical Genetics,1993
5. A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction;Clément;Nature,1998
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