BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

360 related articles for article (PubMed ID: 28281779)

  • 1. Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
    Wang R; Han S; Khan A; Zhang X
    Genet Test Mol Biomarkers; 2017 May; 21(5):316-321. PubMed ID: 28281779
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss.
    Chen Y; Wang Z; Wang Z; Chen D; Chai Y; Pang X; Sun L; Wang X; Yang T; Wu H
    PLoS One; 2015; 10(5):e0127879. PubMed ID: 26011067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
    Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T
    Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
    Doll J; Vona B; Schnapp L; Rüschendorf F; Khan I; Khan S; Muhammad N; Alam Khan S; Nawaz H; Khan A; Ahmad N; Kolb SM; Kühlewein L; Labonne JDJ; Layman LC; Hofrichter MAH; Röder T; Dittrich M; Müller T; Graves TD; Kong IK; Nanda I; Kim HG; Haaf T
    Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33187236
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort.
    Khan A; Han S; Wang R; Ansar M; Ahmad W; Zhang X
    Mol Genet Genomic Med; 2019 Sep; 7(9):e917. PubMed ID: 31389194
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
    Yu X; Lin Y; Xu J; Che T; Li L; Yang T; Wu H
    Orphanet J Rare Dis; 2020 Jan; 15(1):29. PubMed ID: 31992338
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.
    Diaz-Horta O; Duman D; Foster J; Sırmacı A; Gonzalez M; Mahdieh N; Fotouhi N; Bonyadi M; Cengiz FB; Menendez I; Ulloa RH; Edwards YJ; Züchner S; Blanton S; Tekin M
    PLoS One; 2012; 7(11):e50628. PubMed ID: 23226338
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.
    Yang T; Wei X; Chai Y; Li L; Wu H
    Orphanet J Rare Dis; 2013 Jun; 8():85. PubMed ID: 23767834
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Application of next generation sequencing in congenital sensorineural deafness].
    Xu B; Chen Y; Jiang A; Chen C; Wang K; Zheng J; Fu Y
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):811-815. PubMed ID: 29921047
    [No Abstract]   [Full Text] [Related]  

  • 10. Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss.
    Wei Q; Zhu H; Qian X; Chen Z; Yao J; Lu Y; Cao X; Xing G
    J Transl Med; 2014 Nov; 12():311. PubMed ID: 25388789
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
    Richard EM; Santos-Cortez RLP; Faridi R; Rehman AU; Lee K; Shahzad M; Acharya A; Khan AA; Imtiaz A; Chakchouk I; Takla C; Abbe I; Rafeeq M; Liaqat K; Chaudhry T; Bamshad MJ; Nickerson DA; ; Schrauwen I; Khan SN; Morell RJ; Zafar S; Ansar M; Ahmed ZM; Ahmad W; Riazuddin S; Friedman TB; Leal SM; Riazuddin S
    Hum Mutat; 2019 Jan; 40(1):53-72. PubMed ID: 30303587
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.
    Noman M; Ishaq R; Bukhari SA; Ahmed ZM; Riazuddin S
    Genes (Basel); 2019 Dec; 10(12):. PubMed ID: 31835641
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss.
    Choi HJ; Kanwal S; Hameed R; Tamanna N; Perveen S; Mahreen H; Son W; Lee KS; Chung KW
    Genes Genomics; 2023 Feb; 45(2):145-156. PubMed ID: 36472766
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Identification of novel common mutations among patients with non-syndromic hearing loss with high-throughput gene capture technology].
    Zhou Y; Zeng H; Li X; Yang H; Guo W; Hao Z; Li P; Li J; Zhao X; Wang X; Xia L; Ma S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):758-761. PubMed ID: 27984600
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.
    Shang H; Yan D; Tayebi N; Saeidi K; Sahebalzamani A; Feng Y; Blanton S; Liu X
    Biomed Res Int; 2018; 2018():3103986. PubMed ID: 29568747
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.
    Xiang YB; Xu CY; Xu YZ; Li HZ; Zhou LL; Xu XQ; Chen ZH; Tang SH
    Mol Genet Genomic Med; 2020 Dec; 8(12):e1539. PubMed ID: 33095980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
    Liang P; Chen F; Wang S; Li Q; Li W; Wang J; Chen J; Zha D
    Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.
    Deng Y; Sang S; Wen J; Liu Y; Ling J; Chen H; Cai X; Mei L; Chen X; Li M; Li W; Li T; He C; Feng Y
    Int J Pediatr Otorhinolaryngol; 2018 Dec; 115():114-119. PubMed ID: 30368370
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Application of the real-time fluorescence PCR melting curve method in gene screening of non-syndromic hearing loss].
    Liu YL; Jiang XH; Sun J; Mei LY; He CF; Deng YY; Wen J; Feng Y
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Apr; 54(4):286-291. PubMed ID: 30991779
    [No Abstract]   [Full Text] [Related]  

  • 20. Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population.
    Souissi A; Ben Said M; Ben Ayed I; Elloumi I; Bouzid A; Mosrati MA; Hasnaoui M; Belcadhi M; Idriss N; Kamoun H; Gharbi N; Gibriel AA; Tlili A; Masmoudi S
    J Adv Res; 2021 Jul; 31():13-24. PubMed ID: 34194829
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.