Lin N - Search Results

1

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family.

Xu L, Wang X, Li J, Chen L, Wang H, Xu S, Zhang Y, Li W, Yao P, Tan M, Zhou S, Chen M, Pan Y, Chen X, Chen X, Liu Y, Lin N, Huang H, Cao H. Xu L, et al. Among authors: lin n. Clin Genet. 2023 Apr;103(4):413-423. doi: 10.1111/cge.14283. Epub 2023 Jan 12. Clin Genet. 2023. PMID: 36537221

2

A new β-thalassemia deletion mutation [codon 36 (-C)] observed in a Chinese woman.

Huang H, Xu L, Lin N, Xu J, He D, Li Y, Zheng L, Liu H, Lin Y. Huang H, et al. Among authors: lin y, lin n. Hemoglobin. 2010;34(6):599-603. doi: 10.3109/03630269.2010.526841. Hemoglobin. 2010. PMID: 21077770

3

Molecular spectrum of β-thalassemia in Fujian Province, Southeastern China.

Huang H, Xu L, Lin N, He D, Li Y, Guo D, Wang L, Wang Y, Zhen L, Xu J, Lin Y. Huang H, et al. Among authors: lin y, lin n. Hemoglobin. 2013;37(4):343-50. doi: 10.3109/03630269.2013.792274. Epub 2013 May 20. Hemoglobin. 2013. PMID: 23682686

4

[Gene Diagnosis and Analysis of Clinical Hematological Phenotype of Thailand Deleted α-Thalassemia 1].

Lin N, Huang HL, Wang Y, Zheng L, Fang XQ, Cai MY, Wang LS, Liu HK, Xu LP, Lin Y. Lin N, et al. Among authors: lin y. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Aug;24(4):1116-20. doi: 10.7534/j.issn.1009-2137.2016.04.029. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 27531785 Chinese.

5

[Prenatal diagnosis of 22q11 microdeletion syndrome].

Cai M, Huang H, Lin N, Guo N, Wu X, Su L, Xu L. Cai M, et al. Among authors: lin n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):192-195. doi: 10.3760/cma.j.issn.1003-9406.2017.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397216 Chinese.

6

[Prenatal Diagnosis of A Case of SEA-HPFH Deletion Combined with Beta-Thalassemia in A Chinese Family].

Chen MH, Huang HL, Wang Y, Zhang M, Lin N, He DQ, Lin Y, Xu LP. Chen MH, et al. Among authors: lin y, lin n. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Aug;25(4):1142-1146. doi: 10.7534/j.issn.1009-2137.2017.04.032. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017. PMID: 28823283 Chinese.

7

[Prenatal diagnosis of a fetus with Miller-Dieker syndrome].

Xu L, Huang H, Wang Y, An G, Lin N, Zhang M, Wu X, He D, Chen M, Lin Y. Xu L, et al. Among authors: lin y, lin n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):879-883. doi: 10.3760/cma.j.issn.1003-9406.2017.06.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188621 Chinese.

8

Application of the BACs-on-Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions.

Huang H, Zhang M, Wang Y, Lin N, He D, Chen M, Chen L, Lin Y, Xu L. Huang H, et al. Among authors: lin y, lin n. Mol Reprod Dev. 2018 Feb;85(2):146-154. doi: 10.1002/mrd.22945. Epub 2018 Jan 17. Mol Reprod Dev. 2018. PMID: 29247566

9

Optimization of regional median equations of prenatal screening markers for trisomy 21 in a Chinese population.

Xu L, Huang H, Zheng L, He D, Lin N, Wang L, Lin Y. Xu L, et al. Among authors: lin y, lin n. Medicine (Baltimore). 2018 Aug;97(35):e12045. doi: 10.1097/MD.0000000000012045. Medicine (Baltimore). 2018. PMID: 30170416 Free PMC article.

10

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.

Cai M, Huang H, Su L, Lin N, Wu X, Xie X, An G, Li Y, Lin Y, Xu L, Cao H. Cai M, et al. Among authors: lin y, lin n. Mol Cytogenet. 2018 Nov 28;11:58. doi: 10.1186/s13039-018-0408-y. eCollection 2018. Mol Cytogenet. 2018. PMID: 30519285 Free PMC article.

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