Bai ZX - Search Results

1

[Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].

Guo YL, Wang L, Xue SW, Qu SZ, Yang J, Xu H, Bai ZX, Liu N, Kong XD. Guo YL, et al. Among authors: bai zx. Zhonghua Fu Chan Ke Za Zhi. 2018 Jul 25;53(7):464-470. doi: 10.3760/cma.j.issn.0529-567x.2018.07.005. Zhonghua Fu Chan Ke Za Zhi. 2018. PMID: 30078256 Chinese.

2

[Analysis of genetic difference between mild cognitive impairment and Alzheimer's disease through genome-wide association study].

Bai Z, Kong X. Bai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):342-346. doi: 10.3760/cma.j.issn.1003-9406.2018.03.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896728 Chinese.

3

Extension of the mutation spectrum of PAX6 from three Chinese congenital aniridia families and identification of male gonadal mosaicism.

Bai Z, Kong X. Bai Z, et al. Mol Genet Genomic Med. 2018 Nov;6(6):1053-1067. doi: 10.1002/mgg3.481. Epub 2018 Oct 17. Mol Genet Genomic Med. 2018. PMID: 30334364 Free PMC article.

4

[Application of Karyomapping for the prenatal diagnosis of five families affected with facioscapulohumerial muscular dystrophy type 1].

Zheng Y, Kong L, Xu H, Bai Z, Lu Y, Kong X. Zheng Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):203-206. doi: 10.3760/cma.j.issn.1003-9406.2019.03.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835346 Chinese.

5

[Identification of a novel RHO mutation in a pedigree affected with retinitis pigmentosa].

Bai Z, Liu L, Hu S, Wu Q, Kong X. Bai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):234-237. doi: 10.3760/cma.j.issn.1003-9406.2019.03.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835353 Chinese.

6

[X-linked mental retardation combined with autism caused by a novel hemizygous mutation of GRIA3 gene].

Bai Z, Kong X. Bai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):829-833. doi: 10.3760/cma.j.issn.1003-9406.2019.08.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400139 Chinese.

7

[Identification and prenatal diagnosis of a novel NIPBL mutation underlying Cornelia De Lange syndrome].

Bai Z, Kong X. Bai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):910-913. doi: 10.3760/cma.j.issn.1003-9406.2019.09.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515788 Chinese.

8

[Diagnosis of a case with mental retardation due to novel compound heterozygous variants of TRAPPC9 gene].

Bai Z, Kong X. Bai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1115-1119. doi: 10.3760/cma.j.issn.1003-9406.2019.11.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703139 Chinese.

9

[Analysis of a family with recurrent fetal copy number variations in 1p31.1].

Kong X, Zhang T, Bai Z, Su L, Wang L. Kong X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1127-1129. doi: 10.3760/cma.j.issn.1003-9406.2019.11.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703142 Chinese.

10

[Clinical and genetic analysis of an infant with Lowe syndrome caused by exonic duplication of OCRL gene].

Bai Z, Liu L, Hu S, Kong X. Bai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jan 10;37(1):28-32. doi: 10.3760/cma.j.issn.1003-9406.2020.01.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 31922591 Chinese.

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