Wang X - Search Results

1

Dual diagnosis of microcephalic osteosplastic primary dwarfism type II and benign familial infantile seizure type 2: a case report.

Zhu S, Wang J, Zhu H, Wang Q, Tang B, Xiong F, Luo Z, Chen A, Wang X, Leng X, Zeng L. Zhu S, et al. Among authors: wang x, wang j, wang q. Clin Dysmorphol. 2024 Apr 1;33(2):83-86. doi: 10.1097/MCD.0000000000000493. Epub 2024 Feb 6. Clin Dysmorphol. 2024. PMID: 38441202 Free PMC article. No abstract available.

2

[Analysis of 89 amniotic samples using fluorescent in situ hybridization].

Wei P, Li YX, Zeng L, Chen C, Qin SF, Wang XY, Xi N, Tang SQ, Leng M, Liu CL. Wei P, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Apr;30(2):214-7. doi: 10.3760/cma.j.issn.1003-9406.2013.04.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23568739 Chinese.

3

[Detection of chromosomal aneuploidies in spontaneous abortion samples by fluorescence in situ hybridization].

Wei P, Li Y, Chen C, Zeng L, Qin S, Wang X, Xi N. Wei P, et al. Among authors: wang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):229-32. doi: 10.3760/cma.j.issn.1003-9406.2015.02.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25863093 Chinese.

4

[Analysis of genetics mechanism for the phenotypic diversity in a patient carrying a rare ring chromosome 9].

Qin S, Wang X, Li Y, Wei P, Chen C, Zeng L. Qin S, et al. Among authors: wang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Feb;33(1):71-5. doi: 10.3760/cma.j.issn.1003-9406.2016.01.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 26829739 Chinese.

5

[Application of quantitative fluorescencet-PCR in the prenatal diagnosis of chromosomale aneuploidies].

Qin S, Wang X, Chen X, Ye M, Chen C, Wei P, Zeng L, Deng Y, Li Y, Xi N, Song X, Sun L. Qin S, et al. Among authors: wang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):228-231. doi: 10.3760/cma.j.issn.1003-9406.2018.02.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652998 Chinese.

6

[Prenatal diagnosis of a case of Pallister-Killian syndrome].

Song X, Wang X, Deng G, Xi N, Zeng L, Chen C, Sun L, Qin S, Ren Y. Song X, et al. Among authors: wang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jul 10;37(7):771-773. doi: 10.3760/cma.j.issn.1003-9406.2020.07.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32619262 Chinese.

7

Verification of a cryptic t(Y;15) translocation in a male with an apparent 45,X karyotype.

Qin S, Wang X, Wang J, Zhang Z, Chen X, Yin Y, Ye M, Li-Ling J. Qin S, et al. Among authors: wang x, wang j. Mol Cytogenet. 2022 Feb 14;15(1):3. doi: 10.1186/s13039-022-00581-6. Mol Cytogenet. 2022. PMID: 35164811 Free PMC article.

8

Identification of an SRY-negative 46,XX infertility male with a heterozygous deletion downstream of SOX3 gene.

Qin S, Wang X, Wang J. Qin S, et al. Among authors: wang x, wang j. Mol Cytogenet. 2022 Feb 14;15(1):2. doi: 10.1186/s13039-022-00580-7. Mol Cytogenet. 2022. PMID: 35164824 Free PMC article.

9

Delineation of an inverted tandem Xq23-26.3 duplication in a female featuring extremely short stature and mild mental deficiency.

Qin S, Zeng J, Wang J, Ye M, Deng Q, Wang X, Zhang Z, Yi D, Wu Y, Li-Ling J. Qin S, et al. Among authors: wang x, wang j. Mol Cytogenet. 2023 Nov 29;16(1):33. doi: 10.1186/s13039-023-00663-z. Mol Cytogenet. 2023. PMID: 38031145 Free PMC article.

10

Prenatal diagnosis of mosaic chromosomal aneuploidy and uniparental disomy and clinical outcomes evaluation of four fetuses.

Qin S, Wang X, Wang J, Xi N, Yan M, He Y, Ye M, Zhang Z, Yin Y. Qin S, et al. Among authors: wang x, wang j. Mol Cytogenet. 2023 Dec 6;16(1):35. doi: 10.1186/s13039-023-00667-9. Mol Cytogenet. 2023. PMID: 38057902 Free PMC article.

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