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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.
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
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PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I.
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  Data: <searchLink fieldCode="AU" term="%22Rezaei+M%22">Rezaei M</searchLink>; Human Genetics, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Buckett+W%22">Buckett W</searchLink>; Obstetrics and Gynecology, McGill University Health Centre, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Bareke+E%22">Bareke E</searchLink>; McGill University and Génome Québec Innovation Centre, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Surti+U%22">Surti U</searchLink>; Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Majewski+J%22">Majewski J</searchLink>; McGill University and Génome Québec Innovation Centre, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Slim+R%22">Slim R</searchLink>; Human Genetics, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada rima.slim@muhc.mcgill.ca.
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  Data: <searchLink fieldCode="JN" term="%222985087R%22">Journal of medical genetics</searchLink> [J Med Genet] 2022 Jun; Vol. 59 (6), pp. 568-570. <i>Date of Electronic Publication: </i>2021 May 21.
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  Data: Journal Article; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22British+Medical+Association%22">British Medical Association </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>2985087R <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1468-6244 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200222593%22">00222593 </searchLink><i>NLM ISO Abbreviation: </i>J Med Genet <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1136/jmedgenet-2021-107875
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      – Code: eng
        Text: English
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        StartPage: 568
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      – TitleFull: A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I.
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            NameFull: Rezaei M
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            – D: 01
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              Text: 2022 Jun
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              Y: 2022
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              Value: 59
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              Value: 6
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