BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 34589676)

  • 21. First branchial cleft anomalies: otologic manifestations and treatment outcomes.
    Shinn JR; Purcell PL; Horn DL; Sie KC; Manning SC
    Otolaryngol Head Neck Surg; 2015 Mar; 152(3):506-12. PubMed ID: 25524898
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital aural atresia and first branchial cleft anomalies: Cholesteatoma and surgical management.
    Liao EN; Chan DK
    Laryngoscope Investig Otolaryngol; 2022 Jun; 7(3):863-869. PubMed ID: 35734058
    [TBL] [Abstract][Full Text] [Related]  

  • 23. First branchial cleft cyst accompanied by external auditory canal atresia and middle ear malformation: A case report.
    Zhang CL; Li CL; Chen HQ; Sun Q; Liu ZH
    World J Clin Cases; 2020 Aug; 8(16):3616-3620. PubMed ID: 32913872
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Novel Classification System and Surgical Strategies of First Branchial Cleft Anomalies.
    Kong D; Li W; Zhou P; Zhang Y; Dai C
    Laryngoscope; 2024 Apr; ():. PubMed ID: 38676459
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.
    Xu Y; Guan L; Shen T; Zhang J; Xiao X; Jiang H; Li S; Yang J; Jia X; Yin Y; Guo X; Wang J; Zhang Q
    Hum Genet; 2014 Oct; 133(10):1255-71. PubMed ID: 24938718
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosis.
    Chen Y; Zhang Q; Shen T; Xiao X; Li S; Guan L; Zhang J; Zhu Z; Yin Y; Wang P; Guo X; Wang J; Zhang Q
    Invest Ophthalmol Vis Sci; 2013 Jun; 54(6):4351-7. PubMed ID: 23661368
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Atypical first branchial cleft fistula: A case report.
    Chaouki A; Lyoubi M; Lahjaouj M; Rouadi S; Mahtar M
    Int J Surg Case Rep; 2021 Jan; 78():159-161. PubMed ID: 33352445
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
    Lord J; McMullan DJ; Eberhardt RY; Rinck G; Hamilton SJ; Quinlan-Jones E; Prigmore E; Keelagher R; Best SK; Carey GK; Mellis R; Robart S; Berry IR; Chandler KE; Cilliers D; Cresswell L; Edwards SL; Gardiner C; Henderson A; Holden ST; Homfray T; Lester T; Lewis RA; Newbury-Ecob R; Prescott K; Quarrell OW; Ramsden SC; Roberts E; Tapon D; Tooley MJ; Vasudevan PC; Weber AP; Wellesley DG; Westwood P; White H; Parker M; Williams D; Jenkins L; Scott RH; Kilby MD; Chitty LS; Hurles ME; Maher ER;
    Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The identification of novel gene mutations for degenerative lumbar spinal stenosis using whole-exome sequencing in a Chinese cohort.
    Jiang X; Chen D
    BMC Med Genomics; 2021 May; 14(1):134. PubMed ID: 34020649
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The Outcome of Treatment in Second Branchial Cleft Anomalies: A Case Series.
    Paul I; Mohiyuddin SMA; A S; Mohammadi K; Babu P
    Cureus; 2023 Jun; 15(6):e40164. PubMed ID: 37431352
    [TBL] [Abstract][Full Text] [Related]  

  • 32. First branchial cleft anomalies: avoiding the misdiagnosis.
    Kumar R; Sikka K; Sagar P; Kakkar A; Thakar A
    Indian J Otolaryngol Head Neck Surg; 2013 Jul; 65(3):260-3. PubMed ID: 24427578
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Congenital first branchial cleft anomalies in children: a study of 100 surgical cases and a review of the literature.
    Chen W; Xu M; Wang Q; Xu R; Chen J; Xu H; Li X
    Eur Arch Otorhinolaryngol; 2023 Jan; 280(1):425-433. PubMed ID: 36040517
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Whole exome sequencing and analysis of a Chinese family with familial pulmonary sarcoidosis].
    Zhang Q; Huang H; Wang N; Fang CL; Jing XY; Guo J; Sun W; Yu C; Yang XY; Xu ZJ
    Zhonghua Jie He He Hu Xi Za Zhi; 2020 Jun; 43(6):525-531. PubMed ID: 32486560
    [No Abstract]   [Full Text] [Related]  

  • 35. [Exploring the association between
    Chen X; Wang SY; Xue EC; Wang XH; Peng HX; Fan M; Wang MY; Wu YQ; Qin XY; Li J; Wu T; Zhu HP; Li J; Zhou ZB; Chen DF; Hu YH
    Beijing Da Xue Xue Bao Yi Xue Ban; 2022 Jun; 54(3):387-393. PubMed ID: 35701113
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
    Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
    Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Comparison study of whole exome sequencing and targeted panel sequencing in molecular diagnosis of inherited retinal dystrophies].
    Liu XZ; Li YY; Yang LP
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):836-844. PubMed ID: 33047716
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
    Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
    Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis.
    Min BJ; Kang YK; Chung YG; Seo ME; Chang KB; Joo MW
    Clin Orthop Relat Res; 2020 Nov; 478(11):2442-2450. PubMed ID: 32281771
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Branchial cleft and pouch anomalies in childhood: a report of 50 surgical cases.
    Spinelli C; Rossi L; Strambi S; Piscioneri J; Natale G; Bertocchini A; Messineo A
    J Endocrinol Invest; 2016 May; 39(5):529-35. PubMed ID: 26403983
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.