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Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.

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Title: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
Authors: Wu, Jinying1,2 (AUTHOR), Lei, Meifang3 (AUTHOR), Wang, Xuetao1,2 (AUTHOR), Liu, Nan1,2 (AUTHOR), Xu, Xiaowei1,2 (AUTHOR), Gu, Chunyu1,2 (AUTHOR), Yu, Yuping4 (AUTHOR), Liu, Wei5 (AUTHOR) lance_1971@163.com
Source: Italian Journal of Pediatrics. 12/29/2022, Vol. 48 Issue 1, p1-7. 7p.
Database: Academic Search Ultimate
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DbLabel: Academic Search Ultimate
An: 162665380
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  Data: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
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  Data: <searchLink fieldCode="AR" term="%22Wu%2C+Jinying%22">Wu, Jinying</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lei%2C+Meifang%22">Lei, Meifang</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Xuetao%22">Wang, Xuetao</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Nan%22">Liu, Nan</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Xiaowei%22">Xu, Xiaowei</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gu%2C+Chunyu%22">Gu, Chunyu</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yu%2C+Yuping%22">Yu, Yuping</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Wei%22">Liu, Wei</searchLink><relatesTo>5</relatesTo> (AUTHOR)<i> lance_1971@163.com</i>
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  Data: <searchLink fieldCode="JN" term="%22Italian+Journal+of+Pediatrics%22">Italian Journal of Pediatrics</searchLink>. 12/29/2022, Vol. 48 Issue 1, p1-7. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=162665380
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1186/s13052-022-01398-0
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      – Code: eng
        Text: English
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        PageCount: 7
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      – TitleFull: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
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          Name:
            NameFull: Wu, Jinying
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            NameFull: Lei, Meifang
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            NameFull: Wang, Xuetao
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            NameFull: Liu, Nan
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            NameFull: Xu, Xiaowei
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            NameFull: Gu, Chunyu
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            NameFull: Yu, Yuping
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            NameFull: Liu, Wei
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            – D: 29
              M: 12
              Text: 12/29/2022
              Type: published
              Y: 2022
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              Value: 48
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          Titles:
            – TitleFull: Italian Journal of Pediatrics
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