Du J - Search Results

1

X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations.

He WB, Du J, Xie PY, Zhou S, Zhang YX, Lu GX, Lin G, Li W, Tan YQ. He WB, et al. Among authors: du j. Prenat Diagn. 2019 Jul;39(8):603-608. doi: 10.1002/pd.5473. Epub 2019 Jun 3. Prenat Diagn. 2019. PMID: 31069818

2

Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assisted reproductive techniques (ART) in a single center.

Tan Y, Gao Y, Lin G, Fu M, Li X, Yin X, Du J, Li J, Li W, Peng H, Yuan Y, Chen F, Jiang F, Zhang H, Lu G, Gong F, Wang W. Tan Y, et al. Among authors: du j. Prenat Diagn. 2016 Jul;36(7):672-9. doi: 10.1002/pd.4837. Epub 2016 Jun 7. Prenat Diagn. 2016. PMID: 27150972

3

[Genetic testing and prenatal diagnosis of 671 Chinese pedigrees affected with Duchenne/Becker muscular dystrophy].

Luo S, He W, Zhao X, Yang X, Gao B, Li S, Du J, Zhang Q, Tan Y, Lu G, Lin G, Li W. Luo S, et al. Among authors: du j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Sep 10;39(9):925-931. doi: 10.3760/cma.j.cn511374-20210911-00744. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36082559 Chinese.

4

[Progress in the research on cell-free fetal DNA in maternal plasma].

Zhou X, DU J, Lu GX. Zhou X, et al. Among authors: du j. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Oct;11(10):862-5. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19849954 Free article. Review. Chinese. No abstract available.

5

[Study of a family with epidermolysis bullosa simplex resulting from a novel mutation of KRT14 gene].

Meng L, Du J, Li W, Lu G, Tan Y. Meng L, et al. Among authors: du j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):504-508. doi: 10.3760/cma.j.issn.1003-9406.2017.04.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777847 Chinese.

6

Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency.

Yang XW, He WB, Gong F, Li W, Li XR, Zhong CG, Lu GX, Lin G, Du J, Tan YQ. Yang XW, et al. Among authors: du j. Mol Genet Genomic Med. 2018 Mar;6(2):261-267. doi: 10.1002/mgg3.366. Epub 2018 Jan 29. Mol Genet Genomic Med. 2018. PMID: 29378385 Free PMC article.

7

Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.

Yuan SM, Zhang YN, Du J, Li W, Tu CF, Meng LL, Lin G, Lu GX, Tan YQ. Yuan SM, et al. Among authors: du j. Asian J Androl. 2018 Sep-Oct;20(5):473-478. doi: 10.4103/aja.aja_17_18. Asian J Androl. 2018. PMID: 29785970 Free PMC article.

8

XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans.

Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ. Zhang YX, et al. Among authors: du j. Clin Genet. 2019 Mar;95(3):442-443. doi: 10.1111/cge.13475. Epub 2018 Nov 29. Clin Genet. 2019. PMID: 30489636 No abstract available.

9

A rare deep intronic mutation of PKHD1 gene, c.8798-459 C > A, causes autosomal recessive polycystic kidney disease by pseudoexon activation.

Chen J, Ma N, Zhao X, Li W, Zhang Q, Yuan S, Tan YQ, Lu G, Lin G, Du J. Chen J, et al. Among authors: du j. J Hum Genet. 2019 Mar;64(3):207-214. doi: 10.1038/s10038-018-0550-8. Epub 2019 Jan 7. J Hum Genet. 2019. PMID: 30617278

10

Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome.

He WB, Du J, Yang XW, Li W, Tang WL, Dai C, Chen YZ, Zhang YX, Lu GX, Lin G, Gong F, Tan YQ. He WB, et al. Among authors: du j. Reprod Biomed Online. 2019 Mar;38(3):397-406. doi: 10.1016/j.rbmo.2018.11.011. Epub 2018 Dec 8. Reprod Biomed Online. 2019. PMID: 30691934

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