Lan FH - Search Results

1

Further identification of a 140bp sequence from amid intron 9 of human FMR1 gene as a new exon.

Yang WJ, Yan AZ, Xu YJ, Guo XY, Fu XG, Li D, Liao J, Zhang D, Lan FH. Yang WJ, et al. Among authors: lan fh. BMC Genet. 2020 Jun 18;21(1):63. doi: 10.1186/s12863-020-00870-2. BMC Genet. 2020. PMID: 32552710 Free PMC article.

2

[Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I].

Ke LF, Zheng LW, Xie HH, Yan AZ, Zhu ZY, Lan FH. Ke LF, et al. Among authors: lan fh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):50-3. doi: 10.3760/cma.j.issn.1003-9406.2009.01.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19199251 Chinese.

3

[Mutation analysis of SMN gene in a patient and his family with spinal muscular atrophy].

Zeng J, Lin YH, Yan AZ, Cai MY, Ke LF, Lan FH. Zeng J, et al. Among authors: lan fh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):139-43. doi: 10.3760/cma.j.issn.1003-9406.2009.02.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350502 Chinese.

4

[Progress in molecular diagnosis of fragile X syndrome].

Guo XY, Liao J, Lan FH. Guo XY, et al. Among authors: lan fh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Jun;29(3):296-9. doi: 10.3760/cma.j.issn.1003-9406.2012.03.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22678793 Review. Chinese.

5

[Identification of a mosaic mutation of NF1 gene in a sporadic case of neurofibromatosis type 1].

Zhou CY, Li J, Guo XY, Liao J, Wang ZH, Lan FH. Zhou CY, et al. Among authors: lan fh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):529-32. doi: 10.3760/cma.j.issn.1003-9406.2012.05.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042387 Chinese.

6

[Molecular diagnosis and prenatal diagnosis in a hereditary multiple osteochondromas family].

Tang Y, Zheng DZ, Guo XY, Liao J, Lan FH. Tang Y, et al. Among authors: lan fh. Beijing Da Xue Xue Bao Yi Xue Ban. 2013 Dec 18;45(6):906-9. Beijing Da Xue Xue Bao Yi Xue Ban. 2013. PMID: 24343072 Free article. Chinese.

7

Aggregation of Ribosomal Protein S6 at Nucleolus Is Cell Cycle-Controlled and Its Function in Pre-rRNA Processing Is Phosphorylation Dependent.

Zhang D, Chen HP, Duan HF, Gao LH, Shao Y, Chen KY, Wang YL, Lan FH, Hu XW. Zhang D, et al. Among authors: lan fh. J Cell Biochem. 2016 Jul;117(7):1649-57. doi: 10.1002/jcb.25458. Epub 2015 Dec 30. J Cell Biochem. 2016. PMID: 26639987

8

Splicing of exon 9a in FMR1 transcripts results in a truncated FMRP with altered subcellular distribution.

Fu XG, Yan AZ, Xu YJ, Liao J, Guo XY, Zhang D, Yang WJ, Zheng DZ, Lan FH. Fu XG, et al. Among authors: lan fh. Gene. 2020 Mar 20;731:144359. doi: 10.1016/j.gene.2020.144359. Epub 2020 Jan 11. Gene. 2020. PMID: 31935509

9

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.

Tan MQ, Huang WJ, Lan FH, Xu YJ, Zheng MY, Tang Y. Tan MQ, et al. Among authors: lan fh. Biol Reprod. 2022 Jan 13;106(1):108-117. doi: 10.1093/biolre/ioab194. Biol Reprod. 2022. PMID: 34673937

10

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.

Tan MQ, Huang WJ, Lan FH, Xu YJ, Zheng MY, Tang Y. Tan MQ, et al. Among authors: lan fh. Biol Reprod. 2022 Jan 13;106(1):227. doi: 10.1093/biolre/ioab230. Biol Reprod. 2022. PMID: 34904639 No abstract available.

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