Tan J - Search Results

1

Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations.

Yang J, Yuan D, Tan X, Zeng Y, Tang N, Chen D, Tan J, Cai R, Huang J, Yan T. Yang J, et al. Among authors: tan x, tan j. Mol Med Rep. 2022 Feb;25(2):47. doi: 10.3892/mmr.2021.12563. Epub 2021 Dec 8. Mol Med Rep. 2022. PMID: 34878152 Free PMC article.

2

[Molecular diagnosis for a patient with Kennedy disease].

Tan J, Huang S, Wang H, Cai R, Zhao X. Tan J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):754-6. doi: 10.3760/cma.j.issn.1003-9406.2014.06.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449082 Chinese.

3

[An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency].

Tan JQ, Chen DY, Li ZT, Huang JW, Yan TZ, Cai R. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2016 Oct;18(10):1019-1025. doi: 10.7499/j.issn.1008-8830.2016.10.021. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27751224 Free PMC article. Chinese.

4

[Pancytopenia and metabolic decompensation in a neonate].

Tan JQ, Chen DY, Mo ZQ, Li ZT, Huang JW, Cai R, Yan TZ. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2016 Nov;18(11):1150-1153. doi: 10.7499/j.issn.1008-8830.2016.11.019. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27817783 Free PMC article. Chinese.

5

[CPT2 gene mutation analysis and prenatal diagnosis in a family with carnitine palmitoyltransferase II deficiency].

Tan JQ, Chen DY, Li WG, Li ZT, Huang JW, Yan TZ, Cai R. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2016 Dec;18(12):1282-1285. doi: 10.7499/j.issn.1008-8830.2016.12.017. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27974123 Free PMC article. Chinese.

6

[Genetic diagnosis of 10 neonates with primary carnitine deficiency].

Tan JQ, Chen DY, Li ZT, Yan TZ, Huang JW, Cai R. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Nov;19(11):1150-1154. doi: 10.7499/j.issn.1008-8830.2017.11.005. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 29132460 Free PMC article. Chinese.

7

[Clinical and cytogenetic study in a child with de novo chromosome 9 abnormality].

Lu BY, Tan JQ, Yuan DJ, Wang WD, Wei XN, Yan TZ, Cai R. Lu BY, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Jan;20(1):52-55. doi: 10.7499/j.issn.1008-8830.2018.01.011. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 29335083 Free PMC article. Chinese.

8

[Screening for spinal muscular atrophy mutation carriers among 4931 pregnant women from Liuzhou region of Guangxi].

Tan J, Zhang X, Wang Y, Luo S, Yang F, Liu B, Cai R. Tan J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):467-470. doi: 10.3760/cma.j.issn.1003-9406.2018.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098235 Chinese.

9

[Screening indices and their cut-off values for full-term neonates carrying β-thalassemia gene].

Yang JL, Cai R, Chen DY, Tan JQ, Huang LH. Yang JL, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Dec;20(12):990-993. doi: 10.7499/j.issn.1008-8830.2018.12.003. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 30572986 Free PMC article. Chinese.

10

[Clinical and genetic analysis of a child with Noonan syndrome].

Tan J, Li Z, Li W, Liu B, Huang J, Yan T, Huang J, Cai R. Tan J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):588-591. doi: 10.3760/cma.j.issn.1003-9406.2019.06.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055812 Chinese.

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