Jia Z - Search Results

1

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.

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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