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Two cases of 16q12.1q21 deletions and refinement of the critical region.

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Title: Two cases of 16q12.1q21 deletions and refinement of the critical region.
Authors: Apuzzo D; Department of Translational Medicine, Federico II University, Naples, Italy., Cappuccio G; Department of Translational Medicine, Federico II University, Naples, Italy; Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy., Vaisanen T; Department of Clinical Genetics, Turku University Hospital, Turku, Finland., Alagia M; Department of Translational Medicine, Federico II University, Naples, Italy., Pignataro P; Department of Molecular Medicine and Medical Biotechnology, Federico II University, Naples, Italy., Genesio R; Department of Molecular Medicine and Medical Biotechnology, Federico II University, Naples, Italy., Brunetti-Pierri N; Department of Translational Medicine, Federico II University, Naples, Italy; Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy. Electronic address: brunetti@tigem.it.
Source: European journal of medical genetics [Eur J Med Genet] 2020 Jun; Vol. 63 (6), pp. 103878. Date of Electronic Publication: 2020 Feb 08.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Two cases of 16q12.1q21 deletions and refinement of the critical region.
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  Data: <searchLink fieldCode="AU" term="%22Apuzzo+D%22">Apuzzo D</searchLink>; Department of Translational Medicine, Federico II University, Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Cappuccio+G%22">Cappuccio G</searchLink>; Department of Translational Medicine, Federico II University, Naples, Italy; Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Vaisanen+T%22">Vaisanen T</searchLink>; Department of Clinical Genetics, Turku University Hospital, Turku, Finland.<br /><searchLink fieldCode="AU" term="%22Alagia+M%22">Alagia M</searchLink>; Department of Translational Medicine, Federico II University, Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Pignataro+P%22">Pignataro P</searchLink>; Department of Molecular Medicine and Medical Biotechnology, Federico II University, Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Genesio+R%22">Genesio R</searchLink>; Department of Molecular Medicine and Medical Biotechnology, Federico II University, Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Brunetti-Pierri+N%22">Brunetti-Pierri N</searchLink>; Department of Translational Medicine, Federico II University, Naples, Italy; Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy. Electronic address: brunetti@tigem.it.
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  Data: <searchLink fieldCode="JN" term="%22101247089%22">European journal of medical genetics</searchLink> [Eur J Med Genet] 2020 Jun; Vol. 63 (6), pp. 103878. <i>Date of Electronic Publication: </i>2020 Feb 08.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>Netherlands <i>NLM ID: </i>101247089 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1878-0849 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217697212%22">17697212 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Med Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.ejmg.2020.103878
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              Text: 2020 Jun
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              Y: 2020
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