Genetic Mapping Refines DFNB3 to 17p11.2, Suggests Multiple Alleles of DFNB3, and Supports Homology to the Mouse Model shaker-2

References

Page 1

	Year	Citations
A simple salting out procedure for extracting DNA from human nucleated cells S.A. Miller, Dale D. Dykes, Herbert F. Polesky Nucleic Acids Research ChromatinDna SequencingMolecular Biological MethodNatural SciencesNucleic Acid Biochemistry	1988	20.4K
A comprehensive genetic map of the human genome based on 5,264 microsatellites Colette Dib, Sabine Fauré, Cécile Fizames, Nature Genetic AnalysisHaplotype DeterminationMedicineGeneticsEvolutionary Biology	1996	3K
Mutation of human short tandem repeats J. L. Weber, Carmen Chak‐Lui Wong Human Molecular Genetics	1993	1.6K
Faster sequential genetic linkage computations. Robert W. Cottingham, Ramana M. Idury, Alejandro A. Schäffer PubMed	1993	1.4K
A simple and efficient non-organic procedure for the isolation of genomic DNA from blood Jacob I. Grimberg, S. Nawoschik, Leonardo Belluscio, Nucleic Acids Research	1989	516
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells Karen B. Avraham, Tama Hasson, Karen P. Steel, Nature Genetics Knockout MouseWaltzer Deafness GeneMolecular PhysiologyGeneticsUnconventional Myosin	1995	511
Priests and Programmers: Technologies of Power in the Engineered Landscape of Bali. Leo Howe, J. Stephen Lansing Man Architectural DesignEngineered LandscapeReligious SymbolDesignPhilosophy Of Technology	1992	472
Trembler mouse carries a point mutation in a myelin gene Ueli Suter, Andrew A. Welcher, Tayfun Özçelık, Nature Knockout MouseGenetic DisorderNeuroanatomyGeneticsMyelin Gene	1992	422
Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome Ken‐Shiung Chen, Prasad Manian, Thearith Koeuth, Nature Genetics Genetic DisorderHomologous RecombinationGeneticsMolecular GeneticsDisease Gene Identification	1997	384
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2) Frank Greenberg, Richard A. Lewis, Lorraine Potocki, American Journal of Medical Genetics Neurological DisorderDiagnosisPathologyHuman PathologyClinical Genetics	1996	325

Page 1