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Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment Margit Schraders, Laura Ruiz-Palmero, Ersan Kalay, Jaap Oostrik, Francisco J. del Castillo, Orhan Sezgin, Andy J. Beynon, Tim M. Strom, Ronald J.E. Pennings, Celia Zazo Seco, Anne M.M. Oonk, Henricus P.M. Kunst, María Domínguez-Ruiz, Ana M. García-Arumi, Miguel del Campo, Manuela Villamar, Lies H. Hoefsloot, Felipe Moreno, Ronald J.C. Admiraal, Ignacio del Castillo, Hannie Kremer The American Journal of Human Genetics Volume 91, Issue 5, Pages (November 2012) DOI: /j.ajhg Copyright © 2012 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 1 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2012 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 2 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2012 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 3 The American Journal of Human Genetics , DOI: ( /j.ajhg ) Copyright © 2012 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss Kemal O. Yariz, Duygu Duman, Celia Zazo Seco,
Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and.
Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease- Causing Point Mutations Renee P. Stokowski, David R. Cox The American.
Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery Herbert A. Lubs, Roger E. Stevenson, Charles E. Schwartz The American Journal.
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Length Distributions of Identity by Descent Reveal Fine-Scale Demographic History Pier Francesco Palamara, Todd Lencz, Ariel Darvasi, Itsik Pe’er The American.
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Differential Relationship of DNA Replication Timing to Different Forms of Human Mutation and Variation Amnon Koren, Paz Polak, James Nemesh, Jacob J. Michaelson,
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Peopling of Sahul: mtDNA Variation in Aboriginal Australian and Papua New Guinean Populations Alan J. Redd, Mark Stoneking The American Journal of Human.
Replication Stress Induces Genome-wide Copy Number Changes in Human Cells that Resemble Polymorphic and Pathogenic Variants Martin F. Arlt, Jennifer G.
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Novel PMS2 Pseudogenes Can Conceal Recessive Mutations Causing a Distinctive Childhood Cancer Syndrome Michel De Vos, Bruce E. Hayward, Susan Picton, Eamonn.
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Design and Multiseries Validation of a Web-Based Gene Expression Assay for Predicting Breast Cancer Recurrence and Patient Survival Ryan K. Van Laar The.
Telomerase Activity and Expression of Telomerase RNA Component and Telomerase Catalytic Subunit Gene in Cervical Cancer Kenji Nakano, Elizabeth Watney,
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OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin Karlien L.M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze,
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The Importance of the Hook Region of the Cochlea for Bone-Conduction Hearing Namkeun Kim, Charles R. Steele, Sunil Puria Biophysical Journal Volume 107,
Sustained Overexpression of IGF-1 Prevents Age-Dependent Decrease in Charge Movement and Intracellular Ca2+ in Mouse Skeletal Muscle Zhong-Min Wang, María.
Measurement of Relative Copy Number of CDKN2A/ARF and CDKN2B in Bladder Cancer by Real-Time Quantitative PCR and Multiplex Ligation-Dependent Probe Amplification.
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Genetic Parameters and Trends in the Chilean Multibreed Dairy Cattle Population* M.A. Elzo, A. Jara, N. Barria Journal of Dairy Science Volume 87, Issue.
Effects of Milk Powders in Milk Chocolate B. Liang, R.W. Hartel Journal of Dairy Science Volume 87, Issue 1, Pages (January 2004) DOI: /jds.S (04)
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