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Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.

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Title: Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
Authors: Hickey SE; Department of Pediatrics, The Ohio State University College of Medicine, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA. Electronic address: scott.hickey@nationwidechildrens.org., Biswas S, Thrush DL, Pyatt RE, Gastier-Foster JM, Astbury C, Atkin J
Source: European journal of medical genetics [Eur J Med Genet] 2013 Sep; Vol. 56 (9), pp. 521-5. Date of Electronic Publication: 2013 Jul 26.
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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Header DbId: mdl
DbLabel: MEDLINE Ultimate
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AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
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  Data: <searchLink fieldCode="AU" term="%22Hickey+SE%22">Hickey SE</searchLink>; Department of Pediatrics, The Ohio State University College of Medicine, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA. Electronic address: scott.hickey@nationwidechildrens.org.<br /><searchLink fieldCode="AU" term="%22Biswas+S%22">Biswas S</searchLink><br /><searchLink fieldCode="AU" term="%22Thrush+DL%22">Thrush DL</searchLink><br /><searchLink fieldCode="AU" term="%22Pyatt+RE%22">Pyatt RE</searchLink><br /><searchLink fieldCode="AU" term="%22Gastier-Foster+JM%22">Gastier-Foster JM</searchLink><br /><searchLink fieldCode="AU" term="%22Astbury+C%22">Astbury C</searchLink><br /><searchLink fieldCode="AU" term="%22Atkin+J%22">Atkin J</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22101247089%22">European journal of medical genetics</searchLink> [Eur J Med Genet] 2013 Sep; Vol. 56 (9), pp. 521-5. <i>Date of Electronic Publication: </i>2013 Jul 26.
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  Data: Case Reports; Journal Article
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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
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=23895773
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      – Type: doi
        Value: 10.1016/j.ejmg.2013.07.004
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      – Code: eng
        Text: English
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      – TitleFull: Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
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            NameFull: Hickey SE
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            NameFull: Biswas S
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            NameFull: Thrush DL
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            NameFull: Pyatt RE
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            NameFull: Gastier-Foster JM
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            NameFull: Astbury C
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            – D: 01
              M: 09
              Text: 2013 Sep
              Type: published
              Y: 2013
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              Value: 9
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            – TitleFull: European journal of medical genetics
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