Jia Z - Search Results

1

[Genetic analysis of a child with mental retardation and hypospadia].

Ma N, Pang J, Peng Y, Jia Z, Xi H, Liu G, Zhou Y, Wang H. Ma N, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Dec 10;36(12):1199-1202. doi: 10.3760/cma.j.issn.1003-9406.2019.12.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31813147 Chinese.

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 analysis for 2 females carrying idic(Y)(p) and with sex development disorders].

Zhang Y, Wang H, Jia Z, Hu J, Cao W, Tan Y. Zhang Y, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):335-9. doi: 10.3760/cma.j.issn.1003-9406.2016.03.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264816 Chinese.

6

A de novo duplication of chromosome 9q34.13-qter in a fetus with Tetralogy of Fallot Syndrome.

Liu J, Hu H, Ma N, Jia Z, Zhou Y, Hu J, Wang H. Liu J, et al. Among authors: jia z. Mol Cytogenet. 2016 Jul 25;9:54. doi: 10.1186/s13039-016-0267-3. eCollection 2016. Mol Cytogenet. 2016. PMID: 27462370 Free PMC article.

7

Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation: Two case reports and brief literature review.

Yan HM, Hu H, Ahmed A, Feng BB, Liu J, Jia ZJ, Wang H. Yan HM, et al. Medicine (Baltimore). 2017 Nov;96(45):e8549. doi: 10.1097/MD.0000000000008549. Medicine (Baltimore). 2017. PMID: 29137068 Free PMC article. Review.

8

[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.

9

[Prenatal diagnosis of monochorionic-diamniotic twins discordant for 45,X/46,XX mosaicism].

Hu J, Xi H, Ma N, Pang J, Luo Y, Jia Z, Wang H. Hu J, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):260-262. doi: 10.3760/cma.j.issn.1003-9406.2019.03.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835360 Chinese.

10

[Identification of a de novo interstitial 21q22.12q22.13 deletion in a patient with intellectual disability].

Peng Y, Jia Z, Pang J, Hu J, Xi H, Wang H. Peng Y, et al. Among authors: jia z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):704-707. doi: 10.3760/cma.j.issn.1003-9406.2019.07.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302916 Chinese.

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