BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 35076908)

  • 1. [Genetic testing and prenatal diagnosis for thirteen Chinese pedigrees affected with oculocutaneous albinism].
    Yang Y; Mao B; Wang Q; Lie S; Zhang R; Zhao X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Feb; 39(2):143-147. PubMed ID: 35076908
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutational Analysis of TYR, OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism.
    Lin Y; Chen X; Yang Y; Che F; Zhang S; Yuan L; Wu Y
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00687. PubMed ID: 31199599
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism.
    Xu C; Xiang Y; Li H; Xu Y; Mao Y; Zhou L; Xu X; Tang S
    J Clin Lab Anal; 2021 Feb; 35(2):e23647. PubMed ID: 33124154
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Delineating Novel and Known Pathogenic Variants in
    Shakil M; Akbar A; Aisha NM; Hussain I; Ullah MI; Atif M; Kaul H; Amar A; Latif MZ; Qureshi MA; Mahmood S
    Genes (Basel); 2022 Mar; 13(3):. PubMed ID: 35328057
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of Five Novel Variants in Chinese Oculocutaneous Albinism by Targeted Next-Generation Sequencing.
    Qiu B; Ma T; Peng C; Zheng X; Yang J
    Genet Test Mol Biomarkers; 2018 Apr; 22(4):252-258. PubMed ID: 29437493
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mutation analysis of two pedigrees with suspected oculocutaneous albinism].
    Ye H; Lan X; Qiao T; Xu W; Tang X; Yang Y; Zhang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Mar; 36(3):212-216. PubMed ID: 30835348
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation Analysis of 63 Northwest Chinese Probands with Oculocutaneous Albinism.
    Chuan Z; Yan Y; Hao S; Zhang Q; Zhou B; Feng X; Wang X; Liu F; Zheng L; Cao Z; Ma X
    Curr Eye Res; 2021 Jan; 46(1):140-143. PubMed ID: 32552135
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.
    Wang Y; Wang Z; Chen M; Fan N; Yang J; Liu L; Wang Y; Liu X
    PLoS One; 2015; 10(4):e0125651. PubMed ID: 25919014
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations.
    Yang Q; Yi S; Li M; Xie B; Luo J; Wang J; Rong X; Zhang Q; Qin Z; Hang L; Feng S; Fan X
    BMC Med Genet; 2019 Jun; 20(1):106. PubMed ID: 31196117
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism.
    Xiao Y; Zhou C; Xie H; Huang S; Wang J; Liu S
    BMC Genomics; 2022 Apr; 23(1):332. PubMed ID: 35488210
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal genetic diagnosis for two Chinese families affected with oculocutaneous albinism type Ⅱ].
    Hu H; Wang H; Jia Z; Xie Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):424-7. PubMed ID: 25119903
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational Analysis of TYR, OCA2, SLC45A2, and TYRP1 Genes Identifies Novel and Reported Mutations in Chinese Families with Oculocutaneous Albinism.
    Xu B; Chen X; Li H
    Altern Ther Health Med; 2023 Oct; 29(7):278-283. PubMed ID: 37471664
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinism.
    Preising MN; Forster H; Gonser M; Lorenz B
    Mol Vis; 2011 Apr; 17():939-48. PubMed ID: 21541274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Spectrum of pathological genetic variants among 405 Chinese pedigrees affected with oculocutaneous albinism].
    Wang C; Chen C; Zhao X; Zhao G; Liu L; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):725-730. PubMed ID: 32619251
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families.
    Rosenmann A; Bejarano-Achache I; Eli D; Maftsir G; Mizrahi-Meissonnier L; Blumenfeld A
    Prenat Diagn; 2009 Oct; 29(10):939-46. PubMed ID: 19626598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal genotyping of four common oculocutaneous albinism genes in 51 Chinese families.
    Wei AH; Zang DJ; Zhang Z; Yang XM; Li W
    J Genet Genomics; 2015 Jun; 42(6):279-86. PubMed ID: 26165494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families].
    Wu Q; Shi HR; Liu N; Lu N; Jiang M; Zhao ZH; Kong XD
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):377-81. PubMed ID: 22875490
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism.
    Renugadevi K; Sil AK; Perumalsamy V; Sundaresan P
    Mol Vis; 2010 Aug; 16():1514-24. PubMed ID: 20806075
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of a Chinese family with oculocutaneous albinism.
    Wang X; Zhu Y; Shen N; Peng J; Wang C; Liu H; Lu Y
    Oncotarget; 2016 Dec; 7(51):84981-84988. PubMed ID: 27829221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A comprehensive analysis reveals mutational spectra and common alleles in Chinese patients with oculocutaneous albinism.
    Wei A; Wang Y; Long Y; Wang Y; Guo X; Zhou Z; Zhu W; Liu J; Bian X; Lian S; Li W
    J Invest Dermatol; 2010 Mar; 130(3):716-24. PubMed ID: 19865097
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.