Literature DB >> 19339009

Absence of 566C>T mutation in exon 7 of the FSHR gene in Indian women with premature ovarian failure.

Golla Jaya Prakash1, Vishnubhotla Venkata Ravi Kanth, Andrew N Shelling, Roya Rozati, Madireddi Sujatha.   

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Year:  2009        PMID： 19339009     DOI： 10.1016/j.ijgo.2009.01.023

Source DB:  PubMed          Journal:  Int J Gynaecol Obstet        ISSN： 0020-7292            Impact factor:   3.561


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  3 in total

1.  Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure.

Authors:  S Katari; M A Wood-Trageser; H Jiang; E Kalynchuk; R Muzumdar; S A Yatsenko; A Rajkovic
Journal:  J Clin Endocrinol Metab       Date:  2015-04-15       Impact factor: 5.958

2.  "Evaluation of four genes associated with primary ovarian insufficiency in a cohort of Mexican women".

Authors:  K J Juárez-Rendón; J E García-Ortiz
Journal:  J Assist Reprod Genet       Date:  2018-06-18       Impact factor: 3.412

Review 3.  Genetics of primary ovarian insufficiency: new developments and opportunities.

Authors:  Yingying Qin; Xue Jiao; Joe Leigh Simpson; Zi-Jiang Chen
Journal:  Hum Reprod Update       Date:  2015-08-04       Impact factor: 15.610
  3 in total

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