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has been cited by the following articles in journals that are participating in CrossRef's forward linking service: | ||
 |  | A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss Nele Hilgert, Vedat Topsakal, Joost van Dinther, Erwin Offeciers, Paul Van de Heyning, and Guy Van Camp European Journal of Human Genetics (2008) 16: 593 Link to Article |
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| | A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy Montserrat Rodríguez-Ballesteros, Raúl Reynoso, Margarita Olarte, Manuela Villamar, Constantino Morera, Rosamaria Santarelli, Edoardo Arslan, Carme Medá, Carlos Curet, and Christiane Völter Human Mutation (2008) 29: 823 Link to Article |
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| | Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families Muhammad S. Chishti, Attya Bhatti, Sana Tamim, Kwanghyuk Lee, Merry-Lynn McDonald, Suzanne M. Leal, and Wasim Ahmad Journal of Human Genetics (2008) 53: 101 Link to Article |
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| | Ligurian experience on neonatal hearing screening: clinical and epidemiological aspects MG Calevo, P Mezzano, E Zullino, P Padovani, and G Serra Acta Pdiatrica (2007) 96: 1592 Link to Article |
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| | Universal newborn hearing screening: a 27-month experience in the French region of Champagne-Ardenne Marianne Lévêque, Pascal Schmidt, Bernard Leroux, Jean-Baptiste Danvin, Thibault Langagne, Marc Labrousse, and André Chays Acta Pdiatrica (2007) 96: 1150 Link to Article |
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| | Genetic epidemiological studies of congenital/prelingual deafness in Turkey: Population structure and mating type are major determinants of mutation identification Mustafa Tekin and Zehra Serap Arıcı American Journal of Medical Genetics Part A (2007) 143a: 1583 Link to Article |
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| | Carrier Rates of the Ancestral Indian W24X Mutation in GJB2 in the General Gypsy Population and Individual Subisolates Sonja Bouwer, Dora Angelicheva, David Chandler, Pavel Seeman, Ivailo Tournev, and Luba Kalaydjieva Genetic Testing (2007) 11: 455 Link to Article |
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| | A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2–q13.4 E. Kalay, R. Caylan, A. F. Kıroglu, T. Yasar, R. W. J. Collin, J. G. A. M. Heister, J. Oostrik, C. W. R. J. Cremers, H. G. Brunner, and A. Karaguzel Journal of Molecular Medicine (2007) 85: 397 Link to Article |
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| | Reducing False Positives in Newborn Hearing Screening Program Hung-Ching Lin, Min-Tsan Shu, Kuo-Sheng Lee, Huang-Yu Lin, and Grace Lin Otology & Neurotology (2007) 28: 788 Link to Article |
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| | Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic Dinah Yaeger, Jennifer McCallum, Kathy Lewis, Lisa Soslow, Udayan Shah, William Potsic, Catherine Stolle, and Ian D. Krantz American Journal of Medical Genetics Part A (2006) 140a: 827 Link to Article |
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| | DNA sequence analysis ofGJB2, encoding connexin 26: Observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls Hsiao-Yuan Tang, Ping Fang, Patricia A. Ward, Eric Schmitt, Sandra Darilek, Spiros Manolidis, John S. Oghalai, Benjamin B. Roa, and Raye Lynn Alford American Journal of Medical Genetics Part A (2006) 140a: 2401 Link to Article |
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| | Mutations in thelipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss Ersan Kalay, Yun Li, Abdullah Uzumcu, Oya Uyguner, Rob W. Collin, Refik Caylan, Melike Ulubil-Emiroglu, Ferry F.J. Kersten, Gunter Hafiz, and Erwin van Wijk Human Mutation (2006) 27: 633 Link to Article |
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| | A recessive Mendelian model to predict carrier probabilities of DFNB1 for nonsyndromic deafness Juan R. González, Wenyi Wang, Ester Ballana, and Xavier Estivill Human Mutation (2006) 27: 1135 Link to Article |
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| | Auditory status of persons with intellectual disability at the German Special Olympic Games Katrin Neumann, Gabriele Dettmer, Harald Euler, Armin Giebel, Manfred Gross, Gilbert Herer, Sebastian Hoth, Christina Lattermann, and Judy Montgomery International Journal of Audiology (2006) 45: 83 Link to Article |
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| | GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population Rikkert L. Snoeckx, Bulantrisna Djelantik, Lut Van Laer, Paul Van de Heyning, and Guy Van Camp American Journal of Medical Genetics Part A (2005) 135a: 126 Link to Article |
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| | Sequenzielles Neugeborenen-Hörscreening (TEOAE/AABR) reduziert Recall-Rate T. Helge, E. Werle, M. Barnick, C. Wegner, B. Rühe, G. Aust, and R. Rossi HNO (2005) 53: 655 Link to Article |
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| | Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns Tomohiro Oguchi, Akihiro Ohtsuka, Shigenari Hashimoto, Aki Oshima, Satoko Abe, Yumiko Kobayashi, Kyoko Nagai, Tatsuo Matsunaga, Satoshi Iwasaki, and Takashi Nakagawa Journal of Human Genetics (2005) 50: 76 Link to Article |
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| | A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome E. Kalay, A. P. M. Brouwer, R. Caylan, S. B. Nabuurs, B. Wollnik, A. Karaguzel, J. G. A. M. Heister, H. Erdol, F. P. M. Cremers, and C. W. R. J. Cremers Journal of Molecular Medicine (2005) 83: 1025 Link to Article |
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| | GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study R SNOECKX, P HUYGEN, D FELDMANN, S MARLIN, F DENOYELLE, J WALIGORA, M MUELLERMALESINSKA, A POLLAK, R PLOSKI, and A MURGIA The American Journal of Human Genetics (2005) 77: 945 Link to Article |
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| | Comparison of Hearing Screening Programs between One Step with Transient Evoked Otoacoustic Emissions (TEOAE) and Two Steps with TEOAE and Automated Auditory Brainstem Response Hung-Ching Lin, Min-Tsan Shu, Kuo-Sheng Lee, Guan-Min Ho, Tzu-Yu Fu, Sharon Bruna, and Grace Lin The Laryngoscope (2005) 115: 1957 Link to Article |
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| | Outpatient newborn hearing screening Thomas A Littman and Douglas D Backous Cochlear Implants International (2004) 5: 197 Link to Article |
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| | GJB2: The spectrum of deafness-causing allele variants and their phenotype Hela Azaiez, G. Parker Chamberlin, Stephanie M. Fischer, Chelsea L. Welp, Sai D. Prasad, R. Thomas Taggart, Ignacio del Castillo, Guy Van Camp, and Richard J. H. Smith Human Mutation (2004) 24: 305 Link to Article |
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| | Universal newborn hearing screening: fine-tuning the process Kelly A. Baroch Current Opinion in Otolaryngology & Head and Neck Surgery (2003) 11: 424 Link to Article |
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| | Nonsyndromic Hearing Loss Lut Van Laer, Kim Cryns, Richard J. H. Smith, and Guy Van Camp Ear and Hearing (2003) 24: 275 Link to Article |
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| | Early intervention after universal neonatal hearing screening: Impact on outcomes Christine Yoshinaga-Itano Mental Retardation and Developmental Disabilities Research Reviews (2003) 9: 252 Link to Article |
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| | Screening methods: Current status Deborah Hayes Mental Retardation and Developmental Disabilities Research Reviews (2003) 9: 65 Link to Article |
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| | Evidence for Surviving Outer Hair Cell Function in Congenitally Deaf Ears Peter A. Rea and William P. R. Gibson The Laryngoscope (2003) 113: 2030 Link to Article |
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| | Deborah Hayes Current Opinion in Otolaryngology & Head & Neck Surgery (2002) 10: 382 Link to Article |
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| | Current Awareness Pharmacoepidemiology and Drug Safety (2002) 11: 345 Link to Article |
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