The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry

Journal of Clinical Endocrinology and Metabolism

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Main Authors:	Jiang, M., Aittomäki, K., Nilsson, C., Pakarinen, P., Iitiä, A., Torresani, T., Simonsen, H., Goh, V., Pettersson, K., De La Chapelle, A., Huhtaniemi, I.
Other Authors:	OBSTETRICS & GYNAECOLOGY
Format:	Article
Published:	2016
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/133766
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1337662024-11-11T10:22:36Z The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry Jiang, M. Aittomäki, K. Nilsson, C. Pakarinen, P. Iitiä, A. Torresani, T. Simonsen, H. Goh, V. Pettersson, K. De La Chapelle, A. Huhtaniemi, I. OBSTETRICS & GYNAECOLOGY Journal of Clinical Endocrinology and Metabolism 83 12 4338-4343 JCEMA 2016-12-20T08:39:49Z 2016-12-20T08:39:49Z 1998 Article Jiang, M., Aittomäki, K., Nilsson, C., Pakarinen, P., Iitiä, A., Torresani, T., Simonsen, H., Goh, V., Pettersson, K., De La Chapelle, A., Huhtaniemi, I. (1998). The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry. Journal of Clinical Endocrinology and Metabolism 83 (12) : 4338-4343. ScholarBank@NUS Repository. 0021972X http://scholarbank.nus.edu.sg/handle/10635/133766 NOT_IN_WOS
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
description	Journal of Clinical Endocrinology and Metabolism
author2	OBSTETRICS & GYNAECOLOGY
author_facet	OBSTETRICS & GYNAECOLOGY Jiang, M. Aittomäki, K. Nilsson, C. Pakarinen, P. Iitiä, A. Torresani, T. Simonsen, H. Goh, V. Pettersson, K. De La Chapelle, A. Huhtaniemi, I.
format	Article
author	Jiang, M. Aittomäki, K. Nilsson, C. Pakarinen, P. Iitiä, A. Torresani, T. Simonsen, H. Goh, V. Pettersson, K. De La Chapelle, A. Huhtaniemi, I.
spellingShingle	Jiang, M. Aittomäki, K. Nilsson, C. Pakarinen, P. Iitiä, A. Torresani, T. Simonsen, H. Goh, V. Pettersson, K. De La Chapelle, A. Huhtaniemi, I. The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
author_sort	Jiang, M.
title	The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
title_short	The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
title_full	The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
title_fullStr	The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
title_full_unstemmed	The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
title_sort	frequency of an inactivating point mutation (566c → t) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
publishDate	2016
url	http://scholarbank.nus.edu.sg/handle/10635/133766
_version_	1821195590519750656

The frequency of an inactivating point mutation (566C → T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry

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