Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male‐limited precocious puberty
- 18 September 2003
- journal article
- website
- Published by Wiley in Clinical Endocrinology
- Vol. 59 (4) , 533-534
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary–gonadal axis in both sexesClinical Endocrinology, 2000
- A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious pubertyNature, 1993
- Localization of the human luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chromosome 2p21Cytogenetic and Genome Research, 1990