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 *

198 related articles for article (PubMed ID: 26186295)

  • 61. Genetics of pediatric hearing loss: A functional perspective.
    Khela H; Kenna MA
    Laryngoscope Investig Otolaryngol; 2020 Jun; 5(3):511-519. PubMed ID: 32596495
    [TBL] [Abstract][Full Text] [Related]  

  • 62. ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.
    DiStefano MT; Hemphill SE; Oza AM; Siegert RK; Grant AR; Hughes MY; Cushman BJ; Azaiez H; Booth KT; Chapin A; Duzkale H; Matsunaga T; Shen J; Zhang W; Kenna M; Schimmenti LA; Tekin M; Rehm HL; Tayoun ANA; Amr SS;
    Genet Med; 2019 Oct; 21(10):2239-2247. PubMed ID: 30894701
    [TBL] [Abstract][Full Text] [Related]  

  • 63. 50 Years Ago in TheJournalofPediatrics: Genetic Etiology of Syndromic Congenital Hearing Loss.
    Orland MD; Giampietro PF
    J Pediatr; 2022 Jun; 245():38. PubMed ID: 35718381
    [No Abstract]   [Full Text] [Related]  

  • 64. Preimplantation genetic diagnosis: its role in prevention of deafness.
    Taneja MK
    Indian J Otolaryngol Head Neck Surg; 2014 Jan; 66(1):1-3. PubMed ID: 24605291
    [TBL] [Abstract][Full Text] [Related]  

  • 65. The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review.
    Freeman L; Righetti S; Delatycki MB; Scully JL; Kirk EP
    Genet Med; 2022 Sep; 24(9):1803-1813. PubMed ID: 35659827
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Calculation of recurrence risks for heterogeneous genetic disorders.
    Braga MC; Otto PA; Frota-Pessoa O
    Am J Med Genet; 2000 Nov; 95(1):36-42. PubMed ID: 11074492
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss.
    Perry J; Redfield S; Oza A; Rouse S; Stewart C; Khela H; Srinivasan T; Albano V; Shearer E; Kenna M
    Laryngoscope; 2023 Sep; 133(9):2417-2424. PubMed ID: 36515421
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Preimplantation genetic diagnosis and deafness.
    Taneja MK
    Indian J Otolaryngol Head Neck Surg; 2012 Jun; 64(2):103-5. PubMed ID: 23730567
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Effect of Health Education on Knowledge and Behaviour Towards Consanguineous Marriage and Infantile Hearing Loss.
    Thingujam S; Sakthignanavel A; Vengadakrishnan J; Poduval J
    Indian J Otolaryngol Head Neck Surg; 2022 Sep; 74(3):343-349. PubMed ID: 36213470
    [TBL] [Abstract][Full Text] [Related]  

  • 70. A hereditary syndrome with retinopathy and ataxia or deafness in two consanguineous brothers.
    Bitoun P; Bandini D; Rigaudiere F
    Ophthalmic Paediatr Genet; 1991 Sep; 12(3):149-52. PubMed ID: 1754163
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Recessive congenital deafness in a North belgian province.
    DERAEMAEKER R
    Acta Genet Stat Med; 1960; 10():295-304. PubMed ID: 13722007
    [No Abstract]   [Full Text] [Related]  

  • 72. A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia.
    Romanov GP; Pshennikova VG; Lashin SA; Solovyev AV; Teryutin FM; Cherdonova AM; Borisova TV; Sazonov NN; Khusnutdinova EK; Posukh OL; Fedorova SA; Barashkov NA
    PLoS One; 2020; 15(11):e0242219. PubMed ID: 33253245
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Migration between India and Pakistan, 1951-61.
    Visaria PM
    Demography; 1969 Aug; 6(3):323-34. PubMed ID: 21331852
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Genetics & Epigenetics of Hereditary Deafness: An Historical Overview.
    Martini A; Sorrentino F; Sorrentino U; Cassina M
    Audiol Res; 2021 Nov; 11(4):629-635. PubMed ID: 34842610
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Medical genetic evaluation for the etiology of hearing loss in children.
    Smith SD; Kimberling WJ; Schaefer GB; Horton MB; Tinley ST
    J Commun Disord; 1998; 31(5):371-88; quiz 388-9. PubMed ID: 9777485
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Overview of schizophrenia research and treatment in Pakistan.
    Nawaz R; Gul S; Amin R; Huma T; Al Mughairbi F
    Heliyon; 2020 Nov; 6(11):e05545. PubMed ID: 33294688
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Deafness in paediatric age group.
    Chopra H; Munjal M; Gupta SN
    Indian J Otolaryngol Head Neck Surg; 1999 Jul; 51(3):7-10. PubMed ID: 23119536
    [TBL] [Abstract][Full Text] [Related]  

  • 78. A novel loss-of-function mutation in
    Hariharan N; Ravi S; Pradeep BE; Subramanyam KN; Choudhary B; Srinivasan S; Khanchandani P
    Hum Genome Var; 2018; 5():17061. PubMed ID: 29423242
    [TBL] [Abstract][Full Text] [Related]  

  • 79. EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss.
    Dahmani M; Ammar-Khodja F; Bonnet C; Lefèvre GM; Hardelin JP; Ibrahim H; Mallek Z; Petit C
    Orphanet J Rare Dis; 2015 Aug; 10():96. PubMed ID: 26282398
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family.
    Gao J; Wang Q; Dong C; Chen S; Qi Y; Liu Y
    PLoS One; 2015; 10(7):e0133522. PubMed ID: 26196677
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.