HU X - Search Results

1

[Mutation screening of the F VIII gene in 10 hemophilia A families].

LI W, HU X, GAO BD, LI LY, LIAO Y, TANG XM, TANG WL, Lu GX. LI W, et al. Among authors: hu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):127-32. doi: 10.3760/cma.j.issn.1003-9406.2011.02.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21462120 Chinese.

2

[Identification of novel KIT gene mutations in two Chinese families with piebaldism].

He WB, Hu X, Tang WL, Li LY, Lu GX, Li W. He WB, et al. Among authors: hu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):385-8. doi: 10.3760/cma.j.issn.1003-9406.2013.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926000 Chinese.

3

[Study of two Chinese families affected with resistant ovarian syndrome resulted from novel mutations of FSHR gene].

Li W, He W, Zhou L, Hu X, Li S, Gong F, Tan Y. Li W, et al. Among authors: hu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):196-199. doi: 10.3760/cma.j.issn.1003-9406.2017.02.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397217 Chinese.

4

[Genetic analysis of three families affected with split-hand/split-foot malformation].

He W, Lin G, Liang P, Cheng D, Hu X, Zhou L, Xiong B, Tan Y, Lu G, Li W. He W, et al. Among authors: hu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):476-480. doi: 10.3760/cma.j.issn.1003-9406.2017.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777841 Chinese.

5

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency.

He WB, Tan YQ, Hu X, Li W, Xiong B, Luo KL, Gong F, Lu GX, Lin G, Du J. He WB, et al. Among authors: hu x. BMC Med Genet. 2018 Jan 24;19(1):15. doi: 10.1186/s12881-018-0525-9. BMC Med Genet. 2018. PMID: 29368589 Free PMC article.

6

Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism.

Hu X, He WB, Zhang SP, Luo KL, Gong F, Dai J, Zhang Y, Wan ZX, Li W, Yuan SM, Tan YQ, Lu GX, Lin G, Du J. Hu X, et al. Mol Genet Genomic Med. 2021 May;9(5):e1662. doi: 10.1002/mgg3.1662. Epub 2021 May 4. Mol Genet Genomic Med. 2021. PMID: 33942572 Free PMC article.

7

A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.

Xie P, Hu X, Kong L, Mao Y, Cheng D, Kang K, Dai J, Zhao D, Zhang Y, Lu N, Wan Z, Du R, Xiong B, Zhang J, Tan Y, Lu G, Gong F, Lin G, Liang B, Du J, Hu L. Xie P, et al. Among authors: hu x, hu l. Hum Reprod. 2022 Oct 31;37(11):2546-2559. doi: 10.1093/humrep/deac190. Hum Reprod. 2022. PMID: 36066440

8

Reclassification of DMD Duplications as Benign: Recommendations for Cautious Interpretation of Variants Identified in Prenatal Screening.

He W, Meng G, Hu X, Dai J, Liu J, Li X, Hu H, Tan Y, Zhang Q, Lu G, Lin G, Du J. He W, et al. Among authors: hu x, hu h. Genes (Basel). 2022 Oct 28;13(11):1972. doi: 10.3390/genes13111972. Genes (Basel). 2022. PMID: 36360209 Free PMC article.

9

A DMD case caused by X chromosome rearrangement.

Hu H, Yang XW, Cheng DH, Li XR, He WB, Hu X, Gao BD, Zhao XM, Zhang QJ, Du J, Liu JY, Lu GX, Ge L, Li W. Hu H, et al. Among authors: hu x. Yi Chuan. 2023 Jan 20;45(1):88-95. doi: 10.16288/j.yczz.22-179. Yi Chuan. 2023. PMID: 36927641

10

[Genetic analysis and reproductive intervention of 7 families with gonadal mosaicism for Duchenne muscular dystrophy].

Gao B, Yang X, Hu X, He W, Zhao X, Gong F, Du J, Zhang Q, Lu G, Lin G, Li W. Gao B, et al. Among authors: hu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Apr 10;40(4):423-428. doi: 10.3760/cma.j.cn511374-20220525-00351. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36972936 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

32,150 results

Search Page