has been cited by the following articles in journals that are participating in CrossRef's forward linking service: |
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| A novel nonsense mutation inMYO6 is associated with progressive nonsyndromic hearing loss in a DanishDFNA22 family Kirsten M. Sanggaard, Klaus W. Kjaer, Hans Eiberg, Gudrun Nürnberg, Peter Nürnberg, Katrin Hoffman, Hanne Jensen, Charlotte Sørum, Nanna D. Rendtorff, and Lisbeth Tranebjærg American Journal of Medical Genetics Part A (2008) 146a: 1017 Link to Article |
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| MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation Ersan Kalay, Abdullah Uzumcu, Elmar Krieger, Refik Çaylan, Oya Uyguner, Melike Ulubil-Emiroglu, Hidayet Erdol, Hülya Kayserili, Gunter Hafiz, and Nermin Başerer American Journal of Medical Genetics Part A (2007) 143a: 2382 Link to Article |
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| The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3 Quratul Ain, Sabiha Nazli, Saima Riazuddin, Ateeq-ul Jaleel, S. Amer Riazuddin, Ahmad U. Zafar, Shaheen N. Khan, Tayyab Husnain, Andrew J. Griffith, and Zubair M. Ahmed Human Genetics (2007) 122: 445 Link to Article |
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| Non-syndromic, autosomal-recessive deafness MB Petersen and PJ Willems Clinical Genetics (2006) 69: 371 Link to Article |
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| Expression of Myh9 in the mammalian cochlea: Localization within the stereocilia Anand N. Mhatre, Yan Li, Graham Atkin, Abdel Maghnouj, and Anil K. Lalwani Journal of Neuroscience Research (2006) 84: 809 Link to Article |
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| Genetic heterogeneity of deafness phenotypes linked to DFNA4 Tao Yang, Markus Pfister, Nikolaus Blin, Hans P. Zenner, Carsten M. Pusch, and Richard J.H. Smith American Journal of Medical Genetics Part A (2005) 139a: 9 Link to Article |
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| DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1 Jamil Ahmad, Shaheen N. Khan, Shahid Y. Khan, Khushnooda Ramzan, Saima Riazuddin, Zubair M. Ahmed, Edward R. Wilcox, Thomas B. Friedman, and Sheikh Riazuddin Human Genetics (2005) 116: 407 Link to Article |
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| Myosin-1c, the Hair Cell's Adaptation Motor Peter G. Gillespie and Janet L. Cyr Annual Review of Physiology (2004) 66: 521 Link to Article |
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| Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing
Impairment (DFNA4) F DONAUDY, R SNOECKX, M PFISTER, H ZENNER, N BLIN, M DISTAZIO, A FERRARA, C LANZARA, R FICARELLA, and F DECLAU The American Journal of Human Genetics (2004) 74: 770 Link to Article |
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| HUMAN NONSYNDROMIC SENSORINEURAL DEAFNESS* Thomas B. Friedman and Andrew J. Griffith Annual Review of Genomics and Human Genetics (2003) 4: 341 Link to Article |
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| Genetic screening for hearing loss S.W. Hone and R.J.H. Smith Clinical Otolaryngology (2003) 28: 285 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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| GAD2 on Chromosome 10p12 Is a Candidate Gene for Human Obesity Philippe Boutin, Christian Dina, Francis Vasseur, Séverine Dubois, Laetitia Corset, Karin Séron, Lynn Bekris, Janice Cabellon, Bernadette Neve, and Valérie Vasseur-Delannoy PLoS Biology (2003) 1: e8 Link to Article |
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| Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 Z AHMED The American Journal of Human Genetics (2003) 72: 1315 Link to Article |
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| Multiple Mutations ofMYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss F DONAUDY, A FERRARA, L ESPOSITO, R HERTZANO, O BENDAVID, R BELL, S MELCHIONDA, L ZELANTE, K AVRAHAM, and P GASPARINI The American Journal of Human Genetics (2003) 72: 1571 Link to Article |
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| Circadian efferent input toLimulus eyes: Anatomy, circuitry, and impact Barbara-Anne Battelle Microscopy Research and Technique (2002) 58: 345 Link to Article |
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