CrossRef Forward Linking Search Results

This Article:

Tom Walsh, Vanessa Walsh, Sarah Vreugde, Ronna Hertzano, Hashem Shahin, Smadar Haika, Ming K. Lee, Moien Kanaan, Mary-Claire King, and Karen B. Avraham
From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30
PNAS 2002 99: 7518-7523.

has been cited by the following articles in journals that are participating in CrossRef's forward linking service:

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
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
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
Non-syndromic, autosomal-recessive deafness
MB Petersen and PJ Willems
Clinical Genetics (2006) 69: 371
Link to Article
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
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
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
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
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
HUMAN NONSYNDROMIC SENSORINEURAL DEAFNESS*
Thomas B. Friedman and Andrew J. Griffith
Annual Review of Genomics and Human Genetics (2003) 4: 341
Link to Article
Genetic screening for hearing loss
S.W. Hone and R.J.H. Smith
Clinical Otolaryngology (2003) 28: 285
Link to Article
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
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
Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
Z AHMED
The American Journal of Human Genetics (2003) 72: 1315
Link to Article
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
Circadian efferent input toLimulus eyes: Anatomy, circuitry, and impact
Barbara-Anne Battelle
Microscopy Research and Technique (2002) 58: 345
Link to Article