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

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Bibliographic Details
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

Description
ISSN:	1878-0849
DOI:	10.1016/j.ejmg.2020.103878