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A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.

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Title: A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.
Authors: Feichtinger, René G.1 (AUTHOR), Preisel, Martin1 (AUTHOR), Steinbrücker, Katja1 (AUTHOR), Brugger, Karin1 (AUTHOR), Radda, Alexandra2 (AUTHOR), Wortmann, Saskia B.1,3 (AUTHOR) s.wortmann@salk.at, Mayr, Johannes A.1 (AUTHOR)
Source: Genes. Dec2022, Vol. 13 Issue 12, p2191. 6p.
Database: Academic Search Ultimate
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Header DbId: asn
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An: 160986370
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  Data: A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.
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  Data: <searchLink fieldCode="AR" term="%22Feichtinger%2C+René+G%2E%22">Feichtinger, René G.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Preisel%2C+Martin%22">Preisel, Martin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Steinbrücker%2C+Katja%22">Steinbrücker, Katja</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Brugger%2C+Karin%22">Brugger, Karin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Radda%2C+Alexandra%22">Radda, Alexandra</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wortmann%2C+Saskia+B%2E%22">Wortmann, Saskia B.</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<i> s.wortmann@salk.at</i><br /><searchLink fieldCode="AR" term="%22Mayr%2C+Johannes+A%2E%22">Mayr, Johannes A.</searchLink><relatesTo>1</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Genes%22">Genes</searchLink>. Dec2022, Vol. 13 Issue 12, p2191. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=160986370
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        Value: 10.3390/genes13122191
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      – Code: eng
        Text: English
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        PageCount: 6
        StartPage: 2191
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      – TitleFull: A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.
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            NameFull: Preisel, Martin
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            NameFull: Steinbrücker, Katja
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            NameFull: Brugger, Karin
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            NameFull: Radda, Alexandra
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            NameFull: Wortmann, Saskia B.
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            NameFull: Mayr, Johannes A.
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            – D: 01
              M: 12
              Text: Dec2022
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              Y: 2022
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