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. |
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| 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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| ISSN: | 17558794 |
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| DOI: | 10.1186/s12920-023-01631-7 |
