DAFTAR PUSTAKA
Abdullah, A. 2006. Newborn hearing screening: experience in a Malaysian hospital, Singapore Med J, 47(1), pp. 60-6.
Abe S, Usami S, Shinkawa H, Kelley, P,M, Kimberling, W,J. 2000. Prevalent connexin 26 gene (GJB2) mutation in Japanese, J Med Genet. 37, pp. 41-3.
Adler, S,P, Marshall, B,Cy. 2007. Cytomegalovirus Infections, Pediatr Rev. 2007 Mar. 28(3), pp.92-100
Antonio, S,A,M. 2012. Syndromic sensorineural hearing loss. Department of Otolaryngology-Head and Neck Surgery, Eastern Virginia Medical
School, Available from: http://emedicine.medscape.com/article/856116-overview#a0101
(Accesed 30 Maret 2013)
Avraham, K,B, Kanaan, M. 2012. Genomic advances for gene discovery in hereditary hearing loss, J Basic ClinPhysiolPharmacol, 23(3), pp.93-7
Bailey, Byron J, Jonas T, Shawn D. 2006. Genetic Hearing Loss. In: Head and neck surgery–otolaryngology, 4th ed. Lippincott Williams & Wilkins, pp. 1303-16.
Bashiruddin, J. 2009. Newborn Hearing Screening in Six Hospital in Jakarta and Surroundings, Majalah Kedokteran Indonesia, 59 (2), pp.51-4.
Bashiruddin, J. 2010. Pencegahan Gangguan Pendengaran, Tantangan dan Harapan dalam Implementasi Program Sound Hearing 2030, Dalam: Pidato pada Upacara Pengukuhan Sebagai Guru Besar dalam Ilmu Kesehatan Telinga Hidung Tenggorok Kepala dan Leher pada Fakultas Kedokteran Universitas Indonesia.
Ben-salem, S, Rehm,H,L, Willem,P,J, Tamimi, Z,A, Ayadi,H, Ali,B,R, Al-Gazali, L. 2014. Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A, Mol Biol Rep, 41(1), pp.193-200
Berg, A, L, Prieve, B, A, Serpanos, Y, C, & Wheaton, M,A. 2011. Hearing Screening in a Well-Infant Nursery: Propile of Automated ABR-Fail/OAE-Pass, Pediatrics, 127(2), pp. 269-75.
Bhattcharrya, N. 2006. Audiotory Brainstem Response Audiometry. Harvard Medical School, Available from: http//www.emedicene.com. (Accesed 8 Maret 2013)
Bird, P, Botting, A, Milburn, J, Murray D, Heslop, N. 2010. An audit of referrals to the Southern Cochlear Implant Paediatric Programme, The New Zealand Medical Journal, 123(13), pp.10-4
Brownstein, Z, Friedman, L,M, Shahin, H, Oron-Karni, V, Kol, N. 2011. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families’, Genome Biol. 12.p. R89.
Bruzzone & Cohen-Salmon. 2005. Hearing the messenger: Ins(1,4,5)P3 and deafness, Nature Cell Biology 7, pp.14-6.
cochleosaccular mouse model to study 10qter deletions in human deafness, 8(2), pp.23-5
Campbell, K,C,M. 2006. Otoacoustic emissions. Department of Surgery, Division of Otolaryngology, Southern Ilinois University School of
Medicine, Available from:
2012)
Carlson, D, L, Reeh, H,L. 2006. Pediatric audiology, In: Bailey, B.J., Johnson, J.T, Newlands, S.D (eds) Head and neck surgery – otolaryngology. Texas: Lippincott Williams & Wilkins, pp. 1278-88.
Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing, Neurobiol Dis, 73, 418(27)
Choo, D,I, Richter, G,T. 2009. Development of the ear, In: Snow, J.B, Wackyym, P.A. (eds) Ballenger’s otorhinolaryngology head and neck surgery. Connecticut: BC Decker Inc., pp.17-26.
Christopher, P,J. 2005. A Journey Through The Auditory System, In: The Sense of Hearing. Laurence Erlbaum Associates Publishers. London, pp.65-74
2015.
Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan, 79(4), pp.584-90
Coco, M, Salvinelli, F, Greco, F, Trivelli, M, D'Emidio, L, Mesoraca, A, Giorlandino, C, Raffio, R, Coco C. 2013.
deficiency results in reduced retinal activity which is improved by gene therapy, Plos One, 8(8), p. e72027
Cosgrove, D, Zallocchi, M, Binley, K, Lad, Y, Ellis, S, Sylvie W. 2012. Subretinal Delivery of EIAV-based Lentiviral Vectors in the Shaker1 mouse model for Usher Syndrome Type 1B : Development of UshStat, Journal of Clinic Experiment Ophthalmol, 3(2)
Cynthia, C, Morton, Walter, E, Nance. 2006. Newborn Hearing Screening- A Silent Revolution, The New England Journal of Medicine; Massachusetts, 354(20), pp. 2151-64
De Castro, L,S,S, Marinho, A,N,R, Rodrigues, E,M,R, Marques, G,C,T, Carvalho, T,A,A, Silva, L,C,S, Dos Santos, S,E,B. 2013. A study of GJB2 and delGJB6-D13S1830 mutation in Brazillian non-syndromic deaf children from the Amazon region, Braz J Otorhinolaryngol. 79(1), pp.95-9
Deklerck, A,N, Acke, R,A, Janssens, S, De Leenheer, E,M,R. 2015. Etiological Approach in Patients With Unidentified Hearing Loss, International Journal of Pediatric Otorhinolaryngology, 79(2015), pp.216-22.
Deshpande, J,D, Phalke, D,B, Bangal, V,B, Peeyuusha, D, Bhatt, S. 2011. Maternal Risk Factors For Low Birth Weight Neonates: A Hospital Based Case-Control Study In Rural Area Of Western Maharashtra India, National Journal of Community Medicine. 2(3), pp. 394-8
Dhingra, P,L. 2010. Disease of ear, nose, and throat, 4th ed. New Delhi: Elsevier, pp. 3-15.
Diaz, H,O, Duman, D, Foster, J, Sırmacı, A, Gonzalez, M, Mahdieh, N, Fotouhi, N, Bonyadi, M, Cengiz, F, B, Menendez, I, Ulloa, R, H, Edwards, Y, J, Zuchner, S, Blanton, S, Tekin, M. 2012.
Diefendorf, A,O. 2002. Detection and assessment of hearing loss in infants and children, In: Katz J(Ed), Handbook of Clinical Audiology. Lippincot, William & Wilkins, Maryland, Philadelphia, United States of America. Chapter 23, pp. 469-80
Donovalova, G. 2006. Otoacoustic emissions and their use in diagnosing hearing impairment in children, BratislLekListy, 107 (6-7), p.272
Duan, S,H, Zhu, Y,M, Wang, Y,L, Guo, Y,F. 2015.
Duman, D, Sirmaci, A, Cengiz, F,B, Ozdag, H, Tekin. 2011. Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey, Genet Test Mol Biomarkers. 15, pp.29-33
Duman, D, Tekin, M. 2012. Autosomal recessive nonsyndromic deafness genes: a review, Front Biosci. 17, pp. 2213-36
Dzhemileva, L,U, Posukh, O,L, Barashkov, N,A, Fedorova, S,A, Teryutin,F,M, Akhmetova, V,L, Khidiyatova, I,M, Khusainova, R,I, Lobov, S,L, Khusnutdinova, E,K. 2011.
identified exon provides enhancing activity sufficient for normal myo7aa expression in zebrafish sensory hair cells, Dev Neurobiol, 10(1002)
Fang, Y, Gu, M, Wang, C, Suo, F, Wang, G, Xia, Y. 2015.
Feldman, A, S, Grimes, C, T. 1997. Audiologi, In: Ballenger, J.J (ed) Penyakit telinga, hidung, tenggorok, kepala dan leher. Jiliddua. Jakarta: Binarupa Aksara, pp. 273-304
Furutate, S, Iwasaki, S, Nishio, S, Moteki, H, Usami, S. 2011. Clinical Profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord. Acta Oto-Laryngologica, 131(9), pp. 976-82
Gacek, R. 2009. Anatomy of the auditory and vestibular system, In: Snow, J.B, Wackyym, P.A. (eds) Ballenger’s otorhinolaryngology head and neck surgery. Connecticut: BC Decker Inc., pp. 1-15.
Gandia, M, del Castillo, F,J, Rodriguez-Alvarez, F,J, Garrido, G, Villamar, M. 2013. A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment, PLoS ONE, 8(9), pp. 84-8
Geelhoed E,A, Harrison K, Davey A. 2009. Parental perspective of the benefits of genetic testing in children with congenital deafness, Public Health Genomics, Australia, pp. 245-9
Gelfand,S,A. 2010. Conductive mechanism. In: Hearing: an introduction to psychological and physiological acoustics. 5th ed, London: Informa Healthcare, pp. 51-71
Genetic Home Reference. 2013. Available from:
Genetic Evaluation of Congenital Hearing Loss Expert Panel. 2002. Genetics Evaluation Guidelines for the Etiologic, Diagnosis of Congenital Hearing Loss. ACMG Statement, 4(3), pp.162-71
Glasscock, M,E. 2003. Genetics in otology and neurotology, In: Surgery of the ear. 5th ed. BC Decker Inc, pp.121-33
Gomella. 2004. Follow Up of High Risk Infants. Clinical Manual Neonatalogy Management, Procedurs, on Call problems, disease and drugs, Fifth edition. USA: The McGraw Hill, pp.139-43
Guerina, N,G. 1984. Neonatal screening and early treatment for congenital Toxoplasma gondii infection. The new England regional Toxoplasma working group, NEJM. 330, pp. 1858
Guillemin M, Gillam L. 2006. Attitudes to Genetic testing for deafness: The importance of informed choice, Journal of genetic counseling, 15(1), pp.51-8
Gurtler, N. 2008. Hereditary hearing impairment, In: Lalwani, A.K., Ed. Current Diagnosis &Treatment in Otolaryngology Head and Neck surgery. Second edition. USA: The McGraw Hill, 697-704
Hall, A, Pembrey, M, Lutman, M, Steer, C, Bitner, G, M. 2012.
Hall III, J,W, Antonelli, P,J. 2006. Assesment of peripheral and central auditory function, In: bailey et al, B.J., Jonas, J.T, newlands, S.D. (eds) Head &Neck surgery otolaryngology. Philadelphia: Lippincott Williams & Wilkins, pp. 1927-42.
Hamid, M, Karimipoor, M, Chaleshtori, M,H, akbari, M,T. 2009. A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients, Journal of Genetics. 88(3), pp. 359-62
Han, M,Y, Huang, S,S, Wang, G,J, Yuan, Y,Y, Kang, D,Y, Zhang, X, Dai, P. 2011. Zhi, 46(11), pp. 909-13.
Han, M,Y, Lu, Y,P, Bian, X,M, Wang, L,X, Huang, S,S, Wang, G,J, Wang, Y, Kang, D,Y, Zhang, X, Dai, P. 2012. Prenatal genetic test and clinical guidance for 213 hereditary deaf families, 2012. 47(2):127-31
Haraksingh ,R, R, Jahanbani F, Rodriguez-Paris J, Gelernter J, Nadeau KC, Oghalai JS, Schrijver I, Snyder MP. 2014. Genomics, (15), p.1155.
Hearing and Amplification. 2013. Boys town national research hospital. Available from:
HTA Indonesia. 2010. Buku Panduan Tatalaksana Bayi Baru Lahir di Rumah Sakit. 39(9), pp. 538-42
Hu, P, Xie, DH, Xiao, Z,A, Wu,W,J, Ge,S,L, Hu,Z,M, Xia, K. 2004. Mutation screening in selected exons of myosin 7a gene in prelingual non-syndromic hearing impairment patients, 39(9), pp.538-42
dominant mutaion distribution in Chinese deafness patient and the
analysis of phenotype,
Ingber, D,E. 2006. Cellular mechanotransduction: putting all the pieces together again, FASEB J. 20, pp.811-27
Irawan, B. 2008. Genetika molecular, In: Bambang I. (ed) Genetikamolekuler. Cetakan 1, Surabaya: Airlangga, pp. 44-81
Jena N. 2012. DNA damage by reactive species: mechanisms, mutation and repair, J. biosci, 37, pp.503-17.
Ji, Y,B, Han, D,Y, Lan, L, Wang, D,Y, Zong, L, Zhao, FF, Liu Q, Benedict-Alderfer, C, Zheng, Q,Y, Wang, Q,J. 2011. Otolaryngol, 131(2), pp. 124-9.
in ADF/destrin expression in the development of hair cells following Atoh1-induced ectopic regeneration, Exp Ther Med, 6(1),177-183 Joint committee in infant hearing. 2007. Year 2007 position statement:
principles and guidelines for early hearing detection and intervention programs’, Pediatrics, 106(4), pp.789
Jolly, M, Sebire,N, Harris, J, Robinson, S, Regan, L. 2000. The risks associated with pregnancy in women aged 35 years or older, Oxford Journals, 15(11), pp. 2433-7
Kamiya, K. 2015. Inner ear cell therapy targeting hereditary deafness by activation of stem cell homing factors. Front Pharmacol, 6(2), p.2
Kawamoto, K, Ishimoto, S, Minoda, R, Brough, D,E, Raphael, Y. 2003. Math1 Gene Transfer Generates New Cochlear Hair Cells in Mature Guinea Pigs in vivo’, The journal of neuroscience, 23(11), pp. 4395-400
2015. A new compound heterozygous mutation in GJB2
causes nonsyndromic hearing loss in a consanguineous Iranian family.
Kumar, A, Babu, M, Kimberling, W,J, Vankatesh, C,P. 2004. Genetics analysis of a four generation Indian family with usher syndrome: a novel insertion mutation in MYO7A, molecular vision, 10(9), pp. 10-6
Lamershow, S, Hosmer, D,W, Klar, J, Lwangs, S,K. 1997. Besar sampel dalam penelitian kesehatan, Yogyakarta: FK UGM, pp. 1-51
Lattig, M,C, Gelvez, N, Plaza, S,L, Tamayo, G, Uribe. 2008. Deafness on the island of providencia-colombia: different etiology, different genetic counseling, Genetic counseling, 19(4), pp.403-10
Laura, T,L, Abraham, K,L. 2012. Cell Biology, Histology and cell biology.3rd edition. Elsevier. Oxford.
Li, H, Corrales, C,E, Edge, A, Heller, S. 2004. Stem cells as therapy for hearing loss, Trends in molecular medicine, 10(7), pp.309-15
Li, H, Li, Q, Li, H, Chen, Y. 2012. Za Zhi, 26(13), pp. 589-94
Liu, K, C, Cheney, R,E. 2012. 2(5), pp. 158-70.
Liu, F, Li, P, Liu, Y, Li, W, Wong, F, Du, R, Wang, L, Li, C, Jiang, F, Tang, Z, Liu, M. 2013. Novel compound heterozygous mutations in MYO7A in a Chinese family with usher syndrome type 1, Molecular vision. 19, 695-701
Lopponen, T, Dietz, A, Vaisanen, M, L, Valtonen, H, Kosunen, A, Hyvarinen, A, Ignatius, J, Lopponen, H. 2012. Acta Otolaryngol, 132(8):862-73
Lustig, L,R, Lin, D, Venick, H, Larky, J, Yeagle, J, Chinnici, J,
in cochlear implant recipients prevalence and impact on outcome, Arch Otolaryngol Head Neck Surg, 130(5), pp.541-6
Development of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing loss, Dev Neurobiol, 10(1002)
Family influences on the cognitive
development of profoundly deaf children: exploring the effects of socioeconomic status and siblings, 18(4), pp.545-62
Mainley, G,A, Ray, R,R, Popper, A,N. 2008. Otoacoustic emission: active processes and otoacostic emission, Springer, pp. 1-37
McPherson, B, Law, M,M,S, Wong, M,S,M. 2010. Hearing screening for school children: comparison of low-cost, computer-based and conventional audiometry, Child Care Health Dev, 36(3), pp.323-31
Miller, K, A, Williams, L, H, Rose, E, Kuiper, M, Dahl, H, H, Manji, S, S. 2012
Mills, J,H, Khariwala, S,S, Weber, P,C. 2006. Anatomy and physiology of hearing, In: bailey, B,J, Johnson, J,T, Newlands, S,D, (eds) Head and neck surgery – otolaryngology. Texas: Lippincott Williams &wilkins, pp. 900-1887
Mirna, M,S, Mari families with a trimutation in the GJB2 gene causing sensorineural hearing loss, Int J Pediatr Otorhinolaryngol., 79(12), pp. 2295-9. Mohamed, M,R, Alesutan, I, Föller, M, Sopjani, M, Bress, A, Baur, M,
Salama, R,H, Bakr, M,S, Mohamed, M,A, Blin, N, Lang, F, Pfister, M. 2010.
Moller, A,R. 2006. Anatomy of the auditory nervous system, In: Hearing:
anatomy, physiology, and disorders of the auditory system.
Burlington: Elsevier, pp. 80-4
Morton, C,C, Nance, W,E. 2006. Newborn hearing screening-a silent revolution, N Engl J Med. 354, pp. 2151-64
Nikolopoulos, T, P. 2015. Neonatal hearing screening: What we have achieved and what needs to be improved, Int J Pediatr Otorhinolaryngol, 5876(15), pp. 71-3
Nonsyndromic Hearing Loss Cohort: Molecular Epidemiology and Deafness Mutation Spectrum of Patients in Japan, PP.1121-8
Nugroho, D,A, Zulfikar, Muyassaroh. 2012. Kemampuan auditorik anak tuli congenital derajat sangat berat dengan dan tanpa alat bantú dengar, Medica hospitalia, 1(2), pp. 80-2
Okhravi, T, Tarvij, E, S, Hushyar, A, A, Nassirian, H, Najibpour, R. 2015. Evaluation of auditory brain stems evoked response in newborns with pathologic hyperbilirubinemia in mashhad, iran, Iran Red Crescent Med J, 17(2)
Oller, D,K, Eilers, R,E, Neal, A,R, Schwartz, HK. 1999. Precursors to speech in infancy: the prediction of speech and language disorders, Elsevier. 32, pp. 223-45
Parker, M,A, Cheng, Y, F, Kinouchi, H, Bieber, R, Edge, A,S. 2013. An independent construct for conditional expression of atonal homolog-1, Hum Gene Ther Methods, 25(1), pp.1-13
Paulose. 2013. Cochlear implant centre in Jubilee hospital-A dream for the future, Available from:
A
diagnostic paradigm for childhood idiopathic sensorineural hearing loss, 131(6), pp.804-9
Prieve, B,A, Fitzgerald, T,S. 2002. Otoacoustic emissions, In: katz, J. (ed) Handbook of clinical audiology. 5thed. New York: Lippincott Williams &wilkins, pp. 440-63
of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
Rappaport, J,M, Provencal, C. 2002. Neuro-otology for audiologist, In: katz J.(ed) Handbook of clinical audiology. 5thed. New York: Lippincott Williams &wilkins, pp.11-6
Rehm, H,L, Williamson, R,E, Kenna, M,A, Corey, D,P, Korf B,R. 2008. Understanding the genetics of deafness: a guide for patients and families, Harvard Medical School Center for Hereditary Deafness, pp. 1-15
Sang, Q, Yan, X, Wang, H, Feng, R, a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal do minant hearing impairment (DFNA11), Plos One, 8(1), p.e55178
Shahzad, M, Sivakumaran, T,A, Qaiser, T,A, Schuttz, J,M, Hussain, Z, Flanagan, M, Bhinder, M, A, Kissell, D, Greinwald, J,H, Khan, S,N, Friedman, T,B, Zhang, K, Riazuddin, S, Riazuddin,S, Ahmed, Z,M. 2013. Genetic analysis through Otoseq of Pakistani families segregating prelingual hearing loss, OtolaryngolHead Neck Surg. 149(3), pp. 478-87
Shaw, P. 2004. Visual reinforcement audiometry, In Mccormick, b. (ed). Paediatric audiology 0-5 years, 3rd edition. London: Whurr
Sheridan, C. 2011. Gene therapy finds its niche, Nature Biotechnology. 29(2), pp. 121-8
Genetic testing and mutation analysis for the cochlear implantation children and their normal auditory phenotype parents, 26 (19), pp. 874-8
Shin, J,W, Lee, S,C, Lee, H,K, Park, H,J. 2012.
Silva, L,S, Netto, R,C, Sanches, S,G, Carvallo, R,M. 2010.
Sivakumaran, T,A, Husami, A, Kissel, D, Zhang, W, Keddache, M, Black, A,P, Tinkle, B,T, Greinwald, J,H, Jr, Zhang, K. 2013. Performance
evaluation of the next generation sequencing approach for molecular
diagnosis of hereditary hearing loss, OtolaryngolHead NeckSurg. 146(6), pp. 1007-16
[accesed 30 mei 2012]
2014. Apparent phenotypic anticipation in autosomal dominant connexin 26 deafness. J Basic Clin Physiol Pharmacol, 25(3), pp.289-92
environmental factors associated with communication impairments in 9 year old children using an exposome-wide approach, 10(3), pp.23-5
Street, V,A, Li, J, Robbins, C,A, Kallman, J,C. 2011. A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifier, The journal of biological chemistry. 286(17), pp. 15278-86
Steele, D,J, Susman, J, McCurdy, F,A. 2003. Student guide to primary care: making the most of your early clinical experience, Elsevier health sciences, p.370
Steel, K,P. 1999. Connexin 26,Science. 285, pp.1363-4
Sujata, D,E, Archbold, S, Clarke, R. 2007. Investigation and management of the deaf child, In: brown, S.H. (ed) Otorhinolaringology head and neck surgery. 7th ed. Hodder mold, pp. 845-57
Suwento, R, Zizlavsky, S, Hendarmin, H. 2007. Gangguan pendengaran pada bayi dan anak’, In: soepardi, E.A. et al. (eds) Buku ajar ilmu kesehatan telinga hidung tenggorok kepala dan leher. 6th ed. Jakarta: balai penerbit FK UI, pp. 31-42
Tekin, Mustafa, Arnos, Kathleen S, Pandya A. 2001. Advances in hereditary deafness, The lancet, pp. 1082-90
The auditory system. 2011. In: neuroanatomy of the auditory and visual
systems, available from:
Toriello, H,V, Meck, J,M. 2008. Statement on guidance for genetic counseling in advanced paternal age, Genet Med, 10(6), pp. 457-60
Van, D, P, Verkerk, P, H, Van, S, H, L. 2015. Hearing Loss by Week of Gestation and Birth Weight in Very Preterm Neonates, J Pediatr, 3476(14) ,pp. 01210-4
Victor, F, Rosa Andrea, P, Silvia, C,T. 2012. Genetics of congenital deafness next document med clin (Barc), Elsevier. 139, pp. 446-51. Wareing, M,J, Lalwani, A,K, Jackler, R,K. 2006. Development of the ear,
In: Bailey, B,J, Jonas, J,T, Newlands, S,D, (eds) Head & neck surgery otolaryngology. Philadelphia: Lippincott Williams & Wilkins, pp. 1869-80
Wikipedia. 2013. Organ of Corti, Available from:http://en.wikipedia.org/wiki/Organ_of_Corti. [accesed 20 Juli
2014]
Wikipedia. 2015.Restriction fragment length polymorphism, Available from:
Wonkam, A. 2015. Otorhinolaryngol, 79(4), pp. 632-3.
Wright, A. 1997. Anatomy and ultrastructure of the human ear, In: Kerr, A.G. (ed) Scott-Brown’s otolaryngology. Vol.1, London: Butterworth-Heinemann. pp. 1/1/1-10
Wright T, Valentine P. 2008. The anatomy and embryology of the external and middle ear, In: Gleeson, M (Ed) Scott-Brown’s Otorhinolaryngology, Head and Neck Surgery 7th Edition Volume 3. London. Edward Arnold (Publisher) Ltd, pp. 3108
Wu, B,L, Lindeman, N, Lip, V, Adams, A, Amato, R,S, Cox, G. 2002. Effectiveness of sequencing connexin 26 (GJB2) in cases of familial of sporadic childhood deafness referred for molecular diagnostic testing, Genetics In Medicine. 4(4), pp. 279-88
2013. Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment, Plos One, 8(3),p. e57369
Yan, D, Kamiya, K, Ouyang, X,M, Liu, X,Z. 2011. Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice, International Journal of Experimental Pathology. 92, pp. 66–71
Yao, J, Lu, Y, Wei, Q, Cao, X, Xing, G. 2012. p.136.
Yuan, Y, Yu, F, Wang, G, Huang, S, Yu, R, Zhang, X, Huang, D, Han, D, Dai, P. 2010. Prevalence of The GJB2 IVS1+1G >A Mutation In Chinese Hearing Loss Patients With Monoallelic Pathogenic Mutation In The Coding Region of GJB2, Journal of Translational Medicine, 8(127), pp.1-7.
2014. GJB2 c.-23+1G>A
mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss, 23(2), pp.234-8
Zhang, J, Wang, P, Han, B, Ding, Y, Pan, L, Zou, J, Liu, H, Pang, X, Liu, E, Wang, H, Liu, H, Zhang, X, Cheng, X, Feng, D, Li, Q, Wang, D, Zong, L, Yi, Y, Tian, N, Mu, F, Tian, G, Chen, Y, Liu, G, Zhang, F, Yi, X, Yang, L, Wang, Q. 2013. Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China., Int J Pediatr Otorhinolaryngol, 77(12), pp.1929-35.
Zhang, Z, Ding, W, Liu, X, Xu, B, Du, W, Nan, S, Guo, Y. 2012. Otorhinolaryngol, 76(7), pp.984-8.
