Jia Z - Search Results

1

Noninvasive prenatal diagnosis for pregnancies at risk for β-thalassaemia: a retrospective study.

Lv W, Linpeng S, Li Z, Liang D, Jia Z, Meng D, Cram DS, Zhu H, Teng Y, Yin A, Wu L. Lv W, et al. Among authors: jia z. BJOG. 2021 Jan;128(2):448-457. doi: 10.1111/1471-0528.16295. Epub 2020 May 28. BJOG. 2021. PMID: 32363759

2

[Analysis of four fetuses with de novo chromosomal rearrangments using single nucleotide polymorphism microarray chips].

Wang H, Xi H, Jia ZJ, Huang DM, Zhou YC, Wu LQ. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):658-61. doi: 10.3760/cma.j.issn.1003-9406.2012.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225044 Chinese.

3

[Prenatal genetic diagnosis for two Chinese families affected with oculocutaneous albinism type Ⅱ].

Hu H, Wang H, Jia Z, Xie Q. Hu H, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):424-7. doi: 10.3760/cma.j.issn.1003-9406.2014.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119903 Chinese.

4

[Application of next-generation DNA sequencing for prenatal testing of fetal chromosomal aneuploidies].

Liu J, Wang H, Xi H, Jia Z, Zhou Y, Wu L. Liu J, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):533-7. doi: 10.3760/cma.j.issn.1003-9406.2015.04.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252102 Chinese.

5

[Genetic screening and prenatal diagnosis for high risk families of Fragile X syndrome].

Xi H, Zhang Y, Qin L, Kang H, Duan R, Jia Z, Wang H. Xi H, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):653-656. doi: 10.3760/cma.j.issn.1003-9406.2018.05.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30298488 Chinese.

6

Molecular investigation in Chinese patients with primary carnitine deficiency.

Zhang Y, Li H, Liu J, Yan H, Liu Q, Wei X, Xi H, Jia Z, Wu L, Wang H. Zhang Y, et al. Among authors: jia z. Mol Genet Genomic Med. 2019 Sep;7(9):e901. doi: 10.1002/mgg3.901. Epub 2019 Jul 30. Mol Genet Genomic Med. 2019. PMID: 31364285 Free PMC article. Clinical Trial.

7

[Analysis on the Genotype of 5018 Cases of Thalassemia in Hunan Area].

Liu Q, Jia ZJ, Xi H, Liu J, Peng Y, Wang H. Liu Q, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Dec;27(6):1938-1942. doi: 10.19746/j.cnki.issn.1009-2137.2019.06.037. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019. PMID: 31839063 Chinese.

8

Analysis of balanced reciprocal translocations in patients with subfertility using single-molecule optical mapping.

Wang H, Jia Z, Mao A, Xu B, Wang S, Wang L, Liu S, Zhang H, Zhang X, Yu T, Mu T, Xu M, Cram DS, Yao Y. Wang H, et al. Among authors: jia z. J Assist Reprod Genet. 2020 Mar;37(3):509-516. doi: 10.1007/s10815-020-01702-z. Epub 2020 Feb 5. J Assist Reprod Genet. 2020. PMID: 32026199 Free PMC article.

9

Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome.

Liu J, Lin P, Pang J, Jia Z, Peng Y, Xi H, Wu L, Li Z, Wang H. Liu J, et al. Among authors: jia z. Mol Genet Genomic Med. 2020 Aug;8(8):e1313. doi: 10.1002/mgg3.1313. Epub 2020 Jun 15. Mol Genet Genomic Med. 2020. PMID: 32543076 Free PMC article.

10

Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Liu J, Liu Q, Yang S, Ma N, Pang J, Peng Y, Xi H, Jia Z, Luo Y, Jiang M, Teng Y, Yu W, Li Z, Wang H. Liu J, et al. Among authors: jia z. Mol Genet Genomic Med. 2021 Aug;9(8):e1750. doi: 10.1002/mgg3.1750. Epub 2021 Jul 22. Mol Genet Genomic Med. 2021. PMID: 34293831 Free PMC article. Review.

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