Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?

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Title: Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
Authors: Suerink M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Potjer TP; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Versluijs AB; Department of Pediatric Hematology, University Medical Centre, Utrecht, The Netherlands., Ten Broeke SW; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Tops CM; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Wimmer K; Division Human Genetics, Medical University of Innsbruck, Innsbruck, Austria., Nielsen M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Source: Clinical genetics [Clin Genet] 2018 Jan; Vol. 93 (1), pp. 134-137. Date of Electronic Publication: 2017 Sep 15.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
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  Data: <searchLink fieldCode="AU" term="%22Suerink+M%22">Suerink M</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Potjer+TP%22">Potjer TP</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Versluijs+AB%22">Versluijs AB</searchLink>; Department of Pediatric Hematology, University Medical Centre, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Ten+Broeke+SW%22">Ten Broeke SW</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Tops+CM%22">Tops CM</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Wimmer+K%22">Wimmer K</searchLink>; Division Human Genetics, Medical University of Innsbruck, Innsbruck, Austria.<br /><searchLink fieldCode="AU" term="%22Nielsen+M%22">Nielsen M</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
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  Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2018 Jan; Vol. 93 (1), pp. 134-137. <i>Date of Electronic Publication: </i>2017 Sep 15.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE
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              Text: 2018 Jan
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