DOI: 10.1055/s-00000017

Experimental and Clinical Endocrinology & Diabetes

References

Kim HG, Kurth I, Lan F. et al.
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Am J Hum Genet 2008;
83: 511-519

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