2021-YF05-01658-SN/Chengdu Science and Technology Bureau[Grants and Funding] - Search Results

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Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic Anomalies.

Pang Y, Zeng L, Liang H, Cheng C, Shan L, Wang J, Jiang N, Pi G, Yang L, Chen A, Xiong F, Zhu S. Pang Y, et al. Mol Genet Genomic Med. 2024 Sep;12(9):e70005. doi: 10.1002/mgg3.70005. Mol Genet Genomic Med. 2024. PMID: 39225318 Free PMC article.

Prenatal diagnosis of monozygotic twins with phenotypic differences in chromosome 17q12 deletion syndrome.

Ma D, Yuan T, Zhao Z, Zeng L, Wang J, Nie X, Liang H, Pi G, Chen A, Li G, Tang B, Zhu S. Ma D, et al. J Clin Ultrasound. 2024 Nov-Dec;52(9):1495-1498. doi: 10.1002/jcu.23814. Epub 2024 Sep 2. J Clin Ultrasound. 2024. PMID: 39223774

Genetic analysis of partial duplication of the long arm of chromosome 16.

Tang D, Chen A, Xu J, Huang Y, Fan J, Wang J, Zhu H, Pi G, Yang L, Xiong F, Luo Z, Li G, Zeng L, Zhu S. Tang D, et al. BMC Med Genomics. 2024 Dec 23;17(1):294. doi: 10.1186/s12920-024-02059-3. BMC Med Genomics. 2024. PMID: 39716170 Free PMC article.

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