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10. [Inactivating and activating mutations of the human LH/hCG receptor leading to male pseudohermaphroditism and familial male-limited precocious puberty]. Fujieda K; Ito Y Nihon Rinsho; 2002 Feb; 60(2):265-71. PubMed ID: 11857912 [TBL] [Abstract][Full Text] [Related]
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13. Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty. Nagasaki K; Katsumata N; Ogawa Y; Kikuchi T; Uchiyama M Endocr J; 2010; 57(12):1055-60. PubMed ID: 21060208 [TBL] [Abstract][Full Text] [Related]
14. A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty. Kremer H; Martens JW; van Reen M; Verhoef-Post M; Wit JM; Otten BJ; Drop SL; Delemarre-van de Waal HA; Pombo-Arias M; De Luca F; Potau N; Buckler JM; Jansen M; Parks JS; Latif HA; Moll GW; Epping W; Saggese G; Mariman EC; Themmen AP; Brunner HG J Clin Endocrinol Metab; 1999 Mar; 84(3):1136-40. PubMed ID: 10084607 [TBL] [Abstract][Full Text] [Related]
15. Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty. Laue L; Chan WY; Hsueh AJ; Kudo M; Hsu SY; Wu SM; Blomberg L; Cutler GB Proc Natl Acad Sci U S A; 1995 Mar; 92(6):1906-10. PubMed ID: 7892197 [TBL] [Abstract][Full Text] [Related]
16. A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty. Cocco S; Meloni A; Marini MG; Cao A; Moi P Hum Mutat; 1996; 7(2):164-6. PubMed ID: 8829636 [No Abstract] [Full Text] [Related]
17. A missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious puberty. Kraaij R; Post M; Kremer H; Milgrom E; Epping W; Brunner HG; Grootegoed JA; Themmen AP J Clin Endocrinol Metab; 1995 Nov; 80(11):3168-72. PubMed ID: 7593421 [TBL] [Abstract][Full Text] [Related]
18. Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty. Kosugi S; Van Dop C; Geffner ME; Rabl W; Carel JC; Chaussain JL; Mori T; Merendino JJ; Shenker A Hum Mol Genet; 1995 Feb; 4(2):183-8. PubMed ID: 7757065 [TBL] [Abstract][Full Text] [Related]
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