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Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals.

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Title: Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals.
Authors: Owen, Ceris I.1, Bowden, Ramsay2, Parker, Michael J.3, Patterson, Jo3, Patterson, Joan2, Price, Sue4, Sarkar, Ajoy5, Castle, Bruce6, Deshpande, Charulatha7, Splitt, Miranda8, Ghali, Neeti9, Dean, John10, Green, Andrew J.11, Crosby, Charlene12, Deciphering Developmental Disorders Study13, Tatton‐Brown, Katrina12,14, k.tattonbrown@nhs.net
Source: American Journal of Medical Genetics. Part A; May2018, Vol. 176 Issue 5, p1108-1114, 7p
Database: Applied Science & Technology Source
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Header DbId: aci
DbLabel: Applied Science & Technology Source
An: 129235536
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: Extending the phenotype associated with the <italic>CSNK2A1‐</italic>related Okur–Chung syndrome—A clinical study of 11 individuals.
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  Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Medical+Genetics%2E+Part+A%22">American Journal of Medical Genetics. Part A</searchLink>; May2018, Vol. 176 Issue 5, p1108-1114, 7p
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=129235536
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        Value: 10.1002/ajmg.a.38610
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      – Code: eng
        Text: English
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        PageCount: 7
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      – TitleFull: Extending the phenotype associated with the <italic>CSNK2A1‐</italic>related Okur–Chung syndrome—A clinical study of 11 individuals.
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              Text: May2018
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