143 related articles for article (PubMed ID: 31580017)
1. [Genetics of hearing disorders in children].
Paoloni-Giacobino A; Ranza E; Abramowicz M; Senn P; Cao Van H
Rev Med Suisse; 2019 Oct; 15(665):1740-1745. PubMed ID: 31580017
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis, Intervention, and Prevention of Genetic Hearing Loss.
Yang T; Guo L; Wang L; Yu X
Adv Exp Med Biol; 2019; 1130():73-92. PubMed ID: 30915702
[TBL] [Abstract][Full Text] [Related]
3. [Genetic counseling for hearing loss today].
Wang Q; He L
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Jan; 38(1):1-7. PubMed ID: 38297842
[No Abstract] [Full Text] [Related]
4. Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Li MM; Tayoun AA; DiStefano M; Pandya A; Rehm HL; Robin NH; Schaefer AM; Yoshinaga-Itano C;
Genet Med; 2022 Jul; 24(7):1392-1406. PubMed ID: 35802133
[TBL] [Abstract][Full Text] [Related]
5. Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing.
Soares de Lima Y; Chiabai M; Shen J; Córdoba MS; Versiani BR; Benício ROA; Pogue R; Mingroni-Netto RC; Lezirovitz K; Pic-Taylor A; Mazzeu JF; Oliveira SF
Hear Res; 2018 Dec; 370():181-188. PubMed ID: 30390570
[TBL] [Abstract][Full Text] [Related]
6. Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population.
Lee YH; Tsai CY; Lu YS; Lin PH; Chiang YT; Yang TH; Hsu JS; Hsu CJ; Chen PL; Liu TC; Wu CC
Genes (Basel); 2023 Apr; 14(4):. PubMed ID: 37107638
[TBL] [Abstract][Full Text] [Related]
7. High-throughput sequencing to decipher the genetic heterogeneity of deafness.
Brownstein Z; Bhonker Y; Avraham KB
Genome Biol; 2012 May; 13(5):245. PubMed ID: 22647651
[TBL] [Abstract][Full Text] [Related]
8. [Advance in molecular genetic research on X-linked syndromic hearing impairment].
Huang M; Zhang D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):928-933. PubMed ID: 29188633
[TBL] [Abstract][Full Text] [Related]
9. [A review of diagnosis and treatment of syndromic hearing loss].
Liu M; Zhang T
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Mar; 35(3):285-288. PubMed ID: 33794621
[No Abstract] [Full Text] [Related]
10. Evaluation and management of syndromic congenital hearing loss.
Casazza G; Meier JD
Curr Opin Otolaryngol Head Neck Surg; 2017 Oct; 25(5):378-384. PubMed ID: 28697000
[TBL] [Abstract][Full Text] [Related]
11. Whole-exome sequencing and its impact in hereditary hearing loss.
Atik T; Bademci G; Diaz-Horta O; Blanton SH; Tekin M
Genet Res (Camb); 2015 Mar; 97():e4. PubMed ID: 25825321
[TBL] [Abstract][Full Text] [Related]
12. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.
Riga M; Psarommatis I; Lyra Ch; Douniadakis D; Tsakanikos M; Neou P; Apostolopoulos N
Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280
[TBL] [Abstract][Full Text] [Related]
13. The Importance of Early Genetic Diagnostics of Hearing Loss in Children.
Božanić Urbančič N; Battelino S; Tesovnik T; Trebušak Podkrajšek K
Medicina (Kaunas); 2020 Sep; 56(9):. PubMed ID: 32937936
[TBL] [Abstract][Full Text] [Related]
14. Auditory functions in children at schools for the deaf.
Karatas E; Kanlikama M; Mumbuc S
J Natl Med Assoc; 2006 Feb; 98(2):204-10. PubMed ID: 16708506
[TBL] [Abstract][Full Text] [Related]
15. [Attitudes towards prenatal diagnosis of deafness among parents to children with cochlear implants].
Thorsen A; Devantier L; Ovesen T
Ugeskr Laeger; 2009 Apr; 171(17):1387-91. PubMed ID: 19413935
[TBL] [Abstract][Full Text] [Related]
16. Hereditary disturbance of hearing.
Kessler L; Tymnik G
Int J Pediatr Otorhinolaryngol; 1980 Apr; 2(1):63-6. PubMed ID: 6821311
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Aetiologic diagnosis of hearing loss in children identified through newborn hearing screening testing.
Forli F; Giuntini G; Bruschini L; Berrettini S
Acta Otorhinolaryngol Ital; 2016 Feb; 36(1):29-37. PubMed ID: 27054388
[TBL] [Abstract][Full Text] [Related]
19. A stepwise approach to the diagnosis and treatment of hereditary hearing loss.
Tomaski SM; Grundfast KM
Pediatr Clin North Am; 1999 Feb; 46(1):35-48. PubMed ID: 10079788
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members.
Cesca F; Bettella E; Polli R; Cama E; Scimemi P; Santarelli R; Murgia A
Int J Pediatr Otorhinolaryngol; 2018 Jan; 104():88-93. PubMed ID: 29287889
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]