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Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China.

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Title: Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China.
Authors: Yan, Lulu1 (AUTHOR), Cao, Juan2 (AUTHOR), Zhang, Yuxin1 (AUTHOR), Liu, Yingwen1 (AUTHOR), Zou, Jinghui3 (AUTHOR), Lou, Biying4 (AUTHOR), Zhuang, Danyan1 (AUTHOR), Li, Haibo1 (AUTHOR) doctor_lihb075@sina.com
Source: BMC Medical Genomics. 8/17/2023, Vol. 16 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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An: 169995875
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  Data: Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China.
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  Data: <searchLink fieldCode="AR" term="%22Yan%2C+Lulu%22">Yan, Lulu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cao%2C+Juan%22">Cao, Juan</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Yuxin%22">Zhang, Yuxin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Yingwen%22">Liu, Yingwen</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zou%2C+Jinghui%22">Zou, Jinghui</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lou%2C+Biying%22">Lou, Biying</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhuang%2C+Danyan%22">Zhuang, Danyan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Haibo%22">Li, Haibo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> doctor_lihb075@sina.com</i>
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 8/17/2023, Vol. 16 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=169995875
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1186/s12920-023-01631-7
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      – Code: eng
        Text: English
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        PageCount: 8
        StartPage: 1
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      – TitleFull: Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China.
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            NameFull: Yan, Lulu
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            NameFull: Cao, Juan
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            NameFull: Zhang, Yuxin
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            NameFull: Liu, Yingwen
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            NameFull: Zou, Jinghui
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            NameFull: Lou, Biying
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            NameFull: Zhuang, Danyan
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            NameFull: Li, Haibo
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            – D: 17
              M: 08
              Text: 8/17/2023
              Type: published
              Y: 2023
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              Value: 16
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            – TitleFull: BMC Medical Genomics
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