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Another case of holoprosencephaly associated with RAD21 loss-of-function variant.

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Bibliographic Details
Title: Another case of holoprosencephaly associated with RAD21 loss-of-function variant.
Authors: Goel H; Hunter Genetics, Waratah, NSW 2298, Australia., Parasivam G; Hunter Genetics, Waratah, NSW 2298, Australia.
Source: Brain : a journal of neurology [Brain] 2020 Aug 01; Vol. 143 (8), pp. e64.
Publication Type: Letter; Comment
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Editorial & Opinion
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Oxford+University+Press%22">Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>0372537 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2156 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200068950%22">00068950 </searchLink><i>NLM ISO Abbreviation: </i>Brain <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32696056
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      – Type: doi
        Value: 10.1093/brain/awaa173
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      – Code: eng
        Text: English
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        StartPage: e64
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      – TitleFull: Another case of holoprosencephaly associated with RAD21 loss-of-function variant.
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            NameFull: Goel H
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            NameFull: Parasivam G
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            – D: 01
              M: 08
              Text: 2020 Aug 01
              Type: published
              Y: 2020
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              Value: 143
            – Type: issue
              Value: 8
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            – TitleFull: Brain : a journal of neurology
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