These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 27480936)

  • 1. Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic.
    Mehta D; Noon SE; Schwartz E; Wilkens A; Bedoukian EC; Scarano I; Crenshaw EB; Krantz ID
    Am J Med Genet A; 2016 Oct; 170(10):2523-30. PubMed ID: 27480936
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic.
    Yaeger D; McCallum J; Lewis K; Soslow L; Shah U; Potsic W; Stolle C; Krantz ID
    Am J Med Genet A; 2006 Apr; 140(8):827-36. PubMed ID: 16532460
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing?
    Kenna MA; Rehm HL; Robson CD; Frangulov A; McCallum J; Yaeger D; Krantz ID
    Am J Med Genet A; 2007 Jul; 143A(14):1560-6. PubMed ID: 17455295
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic testing for congenital non-syndromic sensorineural hearing loss.
    Raymond M; Walker E; Dave I; Dedhia K
    Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():68-75. PubMed ID: 31163360
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural hearing loss.
    Preciado DA; Lawson L; Madden C; Myer D; Ngo C; Bradshaw JK; Choo DI; Greinwald JH
    Otol Neurotol; 2005 Jul; 26(4):610-5. PubMed ID: 16015155
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A follow-up study of abnormal mutation in neonatal deafness gene screening].
    Liu QM; Tian Y; Yu JJ; He QQ; Peng L; Guo XQ; Li DY; Chen T
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Dec; 54(12):881-887. PubMed ID: 31887812
    [No Abstract]   [Full Text] [Related]  

  • 7. Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort.
    Wener ER; McLennan JD; Papsin BC; Cushing SL; Stavropoulos DJ; Mendoza-Londono R; Quercia N; Gordon KA
    Laryngoscope; 2024 Aug; 134(8):3832-3838. PubMed ID: 38426810
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic Testing Leading to Early Identification of Childhood Ocular Manifestations of Usher Syndrome.
    Brodie KD; Moore AT; Slavotinek AM; Meyer AK; Nadaraja GS; Conrad DE; Weinstein JE; Chan DK
    Laryngoscope; 2021 Jun; 131(6):E2053-E2059. PubMed ID: 33111992
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.
    Xiang J; Jin Y; Song N; Chen S; Shen J; Xie W; Sun X; Peng Z; Sun Y
    BMC Med Genomics; 2022 Jun; 15(1):142. PubMed ID: 35761346
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening for GJB2-R143W-Associated Hearing Impairment: Implications for Health Policy and Practice in Ghana.
    Adadey SM; Quaye O; Amedofu GK; Awandare GA; Wonkam A
    Public Health Genomics; 2020; 23(5-6):184-189. PubMed ID: 33302283
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients.
    Cabanillas R; Diñeiro M; Cifuentes GA; Castillo D; Pruneda PC; Álvarez R; Sánchez-Durán N; Capín R; Plasencia A; Viejo-Díaz M; García-González N; Hernando I; Llorente JL; Repáraz-Andrade A; Torreira-Banzas C; Rosell J; Govea N; Gómez-Martínez JR; Núñez-Batalla F; Garrote JA; Mazón-Gutiérrez Á; Costales M; Isidoro-García M; García-Berrocal B; Ordóñez GR; Cadiñanos J
    BMC Med Genomics; 2018 Jul; 11(1):58. PubMed ID: 29986705
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss.
    Lenarduzzi S; Morgan A; Faletra F; Cappellani S; Morgutti M; Mezzavilla M; Peruzzi A; Ghiselli S; Ambrosetti U; Graziano C; Seri M; Gasparini P; Girotto G
    Hear Res; 2019 Sep; 381():107769. PubMed ID: 31387071
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Newborn hearing screening and genetic testing in 8974 Brazilian neonates.
    Nivoloni Kde A; da Silva-Costa SM; Pomílio MC; Pereira T; Lopes Kde C; de Moraes VC; Alexandrino F; de Oliveira CA; Sartorato EL
    Int J Pediatr Otorhinolaryngol; 2010 Aug; 74(8):926-9. PubMed ID: 20538352
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SOX10 mutations mimic isolated hearing loss.
    Pingault V; Faubert E; Baral V; Gherbi S; Loundon N; Couloigner V; Denoyelle F; Noël-Pétroff N; Ducou Le Pointe H; Elmaleh-Bergès M; Bondurand N; Marlin S
    Clin Genet; 2015 Oct; 88(4):352-9. PubMed ID: 25256313
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nonsyndromic hereditary hearing loss.
    Alford RL
    Adv Otorhinolaryngol; 2011; 70():37-42. PubMed ID: 21358183
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Outcomes of Gene Panel Testing for Sensorineural Hearing Loss in a Diverse Patient Cohort.
    Liao EN; Taketa E; Mohamad NI; Chan DK
    JAMA Netw Open; 2022 Sep; 5(9):e2233441. PubMed ID: 36166228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hearing Impairment Overview in Africa: the Case of Cameroon.
    Wonkam Tingang E; Noubiap JJ; F Fokouo JV; Oluwole OG; Nguefack S; Chimusa ER; Wonkam A
    Genes (Basel); 2020 Feb; 11(2):. PubMed ID: 32098311
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Towards an etiologic diagnosis: assessing the patient with hearing loss.
    Jerry J; Oghalai JS
    Adv Otorhinolaryngol; 2011; 70():28-36. PubMed ID: 21358182
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach.
    Wang J; Xiang J; Chen L; Luo H; Xu X; Li N; Cui C; Xu J; Song N; Peng J; Peng Z
    Sci Rep; 2021 Feb; 11(1):4036. PubMed ID: 33597575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.