Literature DB >> 34021051

A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I.

Maryam Rezaei1, William Buckett2, Eric Bareke3, Urvashi Surti4, Jacek Majewski3, Rima Slim5.   

Abstract

Entities:  

Keywords:  DNA; genetics; molecular biology; sequence analysis; women's health

Mesh:

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Year:  2021        PMID: 34021051     DOI: 10.1136/jmedgenet-2021-107875

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  2 in total

1.  Recurrent pregnancy loss in mice lacking the X-linked Ccnb3 gene†.

Authors:  Jessica Y Chotiner; N Adrian Leu; Yang Xu; P Jeremy Wang
Journal:  Biol Reprod       Date:  2022-03-19       Impact factor: 4.161

2.  Identification of genetic polymorphisms in unexplained recurrent spontaneous abortion based on whole exome sequencing.

Authors:  Jiang-Tao Mou; Shi-Xing Huang; Li-Li Yu; Jing Xu; Qiao-Ling Deng; Yi-Shan Xie; Kun Deng
Journal:  Ann Transl Med       Date:  2022-05
  2 in total

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