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Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a lowfrequency noncoding RBM8A SNP: a new familial case.

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Title: Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a lowfrequency noncoding RBM8A SNP: a new familial case.
Authors: Tassano, Elisa1 eli.tassano@gmail.com, Gimelli, Stefania2, Divizia, Maria Teresa3, Lerone, Margherita3, Vaccari, Carlotta4, Puliti, Aldamaria3,4, Gimelli, Giorgio1
Source: Molecular Cytogenetics (17558166). 11/5/2015, Vol. 8, p1-7. 7p.
Database: Academic Search Ultimate
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  Data: Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a lowfrequency noncoding RBM8A SNP: a new familial case.
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  Data: <searchLink fieldCode="JN" term="%22Molecular+Cytogenetics+%2817558166%29%22">Molecular Cytogenetics (17558166)</searchLink>. 11/5/2015, Vol. 8, p1-7. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=110843957
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        Value: 10.1186/s13039-015-0188-6
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      – TitleFull: Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a lowfrequency noncoding RBM8A SNP: a new familial case.
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              Text: 11/5/2015
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