A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I.
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| Title: | A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I. |
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| Authors: | Rezaei M; Human Genetics, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada., Buckett W; Obstetrics and Gynecology, McGill University Health Centre, Montréal, Québec, Canada., Bareke E; McGill University and Génome Québec Innovation Centre, Montréal, Québec, Canada., Surti U; Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA., Majewski J; McGill University and Génome Québec Innovation Centre, Montréal, Québec, Canada., Slim R; Human Genetics, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada rima.slim@muhc.mcgill.ca. |
| Source: | Journal of medical genetics [J Med Genet] 2022 Jun; Vol. 59 (6), pp. 568-570. Date of Electronic Publication: 2021 May 21. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1468-6244 |
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| DOI: | 10.1136/jmedgenet-2021-107875 |
