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SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.

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Title: SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.
Authors: Bukowska-Olech, Ewelina1 (AUTHOR) ewe.olech@gmail.com, Sowińska-Seidler, Anna1 (AUTHOR), Wierzba, Jolanta2 (AUTHOR), Jamsheer, Aleksander1,3 (AUTHOR) jamsheer@wp.pl
Source: Orphanet Journal of Rare Diseases. 8/26/2022, Vol. 17 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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  Data: SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.
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  Data: <searchLink fieldCode="AR" term="%22Bukowska-Olech%2C+Ewelina%22">Bukowska-Olech, Ewelina</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> ewe.olech@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Sowińska-Seidler%2C+Anna%22">Sowińska-Seidler, Anna</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wierzba%2C+Jolanta%22">Wierzba, Jolanta</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jamsheer%2C+Aleksander%22">Jamsheer, Aleksander</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<i> jamsheer@wp.pl</i>
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 8/26/2022, Vol. 17 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=158784589
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        Value: 10.1186/s13023-022-02480-w
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      – Code: eng
        Text: English
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      – TitleFull: SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.
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            NameFull: Bukowska-Olech, Ewelina
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            NameFull: Sowińska-Seidler, Anna
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            NameFull: Wierzba, Jolanta
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            NameFull: Jamsheer, Aleksander
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            – D: 26
              M: 08
              Text: 8/26/2022
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              Y: 2022
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