Zhang Y - Search Results

1

A case report of a novel HIST1H1E mutation and a review of the bibliography to evaluate the genotype-phenotype correlations.

Zhao W, Zhang Y, Lv T, He J, Zhu B. Zhao W, et al. Among authors: zhang y. Mol Genet Genomic Med. 2023 Dec;11(12):e2273. doi: 10.1002/mgg3.2273. Epub 2023 Aug 21. Mol Genet Genomic Med. 2023. PMID: 37605493 Free PMC article. Review.

2

[A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].

Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH. Zhu BS, et al. Zhonghua Fu Chan Ke Za Zhi. 2012 Feb;47(2):85-9. Zhonghua Fu Chan Ke Za Zhi. 2012. PMID: 22455737 Chinese.

3

[Analysis of neonatal screening results for congenital hypothyroidism in parts of Yunnan Province, China].

Zhang YH, Li L, Chen H, Zhu S, Zhang J, Li SY, Wang RH, Zhu BS. Zhang YH, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Jan;17(1):45-8. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 25616292 Free article. Chinese.

4

[Mutations of phenylalanine hydroxylase gene detected in 20 patients with phenylketonuria from Yunnan Province].

Tang X, Chen H, Zhang Y, Li L, Mi H, Xu Q, Zhu B. Tang X, et al. Among authors: zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):153-7. doi: 10.3760/cma.j.issn.1003-9406.2015.02.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25863075 Chinese.

5

Prevalence of hemoglobin E in Yunnan Province of Southwest China.

He J, Zeng X, Zhang Y, Su J, Ding X, Li S, Xu Y, Pu J, Jin C, Zhu B. He J, et al. Among authors: zhang y. Hematology. 2016 Jan;21(1):54-9. doi: 10.1179/1607845415Y.0000000044. Epub 2015 Aug 20. Hematology. 2016. PMID: 26292035 Free article.

6

[Gene Analysis of Thalassemia in Han and Dai Ethnic Childbearing-aged Population of Chinese Yunnan Province].

He J, Zeng XH, Xu YM, Pu J, Zhou FZ, Jin CC, Su J, Zhang JM, Chen H, Zhang J, Li SY, Zhang YH, Zhu BS. He J, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Feb;24(1):150-6. doi: 10.7534/j.issn.1009-2137.2016.01.029. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 26913412 Chinese.

7

[Application of BoBs technique for detecting common chromosome microdeletion and microduplication syndromes].

Yang B, Tang X, Su J, Chen H, Zhang J, Yin Y, Feng Y, Zhang Y, Zhu S, Zhang J, Zhu B. Yang B, et al. Among authors: zhang j, zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):452-7. doi: 10.3760/cma.j.issn.1003-9406.2016.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27454996 Chinese.

8

[Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China].

Yang JH, Zhang JH, Zhang YH, Xu XZ, Chen H, Li Y, Jiang Y, Wang Z, Zhu BS, Li L. Yang JH, et al. Among authors: zhang jh, zhang yh. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jul;19(7):741-747. doi: 10.7499/j.issn.1008-8830.2017.07.003. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28697824 Free PMC article. Chinese.

9

[Genetic analysis and prenatal diagnosis for a pregnant woman with an unbalanced t(1;2), t(6;7) translocation and intellectual disability].

Zhang Y, Yang B, Tang X, Chen S, Yu R, He J, Su J, Zhu S, Zhu B. Zhang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):583-587. doi: 10.3760/cma.j.issn.1003-9406.2017.04.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777864 Chinese.

10

Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23.

Bai B, Guo YR, Zhang YH, Jin CC, Zhang JM, Chen H, Zhu BS. Bai B, et al. Chin Med J (Engl). 2019 Mar 5;132(5):600-603. doi: 10.1097/CM9.0000000000000100. Chin Med J (Engl). 2019. PMID: 30807358 Free PMC article. No abstract available.

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