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المؤلفون: Bethany T. Neilson, Tyler V. King, Douglas L. Kane, L. D. Overbeck
المصدر: Hydrological Processes. 34:633-648
مصطلحات موضوعية: Hydrology, geography, Watershed, geography.geographical_feature_category, 010504 meteorology & atmospheric sciences, Discharge, Coastal plain, 0207 environmental engineering, Climate change, 02 engineering and technology, Permafrost, 01 natural sciences, Arctic, Environmental science, Precipitation, 020701 environmental engineering, Surface runoff, 0105 earth and related environmental sciences, Water Science and Technology
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2
المؤلفون: Tyler V. King, Bethany T. Neilson, L. D. Overbeck, Douglas L. Kane
المصدر: Water Resources Research. 52:4358-4376
مصطلحات موضوعية: geography, geography.geographical_feature_category, 010504 meteorology & atmospheric sciences, 0208 environmental biotechnology, 02 engineering and technology, Sensible heat, Energy budget, 01 natural sciences, 020801 environmental engineering, Arctic, Heat flux, Climatology, Latent heat, Heat transfer, Tributary, Environmental science, Shortwave radiation, 0105 earth and related environmental sciences, Water Science and Technology
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3
المؤلفون: Eugene R. Zabarovsky, George Klein, Bi Fang Li, Su Fang Yao, James D. Eudy, Ji Yi Wang, Eva Uzvolgyi, Philip M. Kelley, Janos Sumegi, Michael D. Weston, L. D. Overbeck, Dong Kai Zhen, William J. Kimberling, Catherine B. Talmadge, Manling Ma-Edmonds, Eric J. Stanbridge, Peter Berglund
المصدر: Genomics. 35:79-86
مصطلحات موضوعية: Yeast artificial chromosome, Usher syndrome, Molecular Sequence Data, Genes, Recessive, Locus (genetics), Deafness, Biology, Sequence-tagged site, Chromosome Walking, Genetic Heterogeneity, Gene mapping, Image Processing, Computer-Assisted, otorhinolaryngologic diseases, Genetics, medicine, Humans, Chromosomes, Artificial, Yeast, In Situ Hybridization, Fluorescence, Sequence Tagged Sites, Base Sequence, Contig, Syndrome, medicine.disease, Chromosomes, Human, Pair 1, Genetic marker, Microsatellite, Retinitis Pigmentosa
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4
المؤلفون: Richard J.H. Smith, A. M. Brower, Claes Möller, J. A. Grunkemeyer, D. J. Blackwood, L. D. Overbeck, Denise M. Hoover, Peter Beighton, S. Pieke Dahl, Michael D. Weston, P. Rowland, William Reardon, I. A. Priluck, S. Davenport, J. B. Kenyon, Jacquie Greenberg, William J. Kimberling
المصدر: Genomics. 14:988-994
مصطلحات موضوعية: Male, Positional cloning, Genetic Linkage, Usher syndrome, Molecular Sequence Data, Oligonucleotides, Locus (genetics), Biology, Gene mapping, Retinitis pigmentosa, otorhinolaryngologic diseases, Genetics, medicine, Humans, Hearing Disorders, Gene, Base Sequence, Chromosomes, Human, Pair 11, Usher Syndrome Type 1, Chromosome Mapping, Syndrome, medicine.disease, eye diseases, Pedigree, Genetic marker, Female, Lod Score, Retinitis Pigmentosa
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5
المؤلفون: J. B. Kenyon, William J. Kimberling, Hideichi Shinkawa, Satoshi Horai, Satoko Abe, Shin-ichi Usami, L. D. Overbeck, Denise M. Hoover, Michael D. Weston
المصدر: European journal of human genetics : EJHG. 6(6)
مصطلحات موضوعية: Genetics, Mitochondrial DNA, Phylogenetic tree, Hearing loss, Hearing Loss, Sensorineural, Biology, medicine.disease, DNA, Mitochondrial, Pedigree, Restriction enzyme, D-loop, Japan, Mutation (genetic algorithm), Mutation, medicine, Humans, Sensorineural hearing loss, Restriction fragment length polymorphism, medicine.symptom, Genetics (clinical), Phylogeny, Polymorphism, Restriction Fragment Length
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3531d190a0674cdef1d2099355803f30
https://pubmed.ncbi.nlm.nih.gov/9887373 -
6
المؤلفون: Mark S. Mooseker, Zheng-Yi Chen, David P. Corey, Tama Hasson, Philip M. Kelley, Michael D. Weston, Janos Sumegi, Paul S. Ing, William J. Kimberling, Catherine B. Talmadge, Dana J. Orten, L. D. Overbeck, Jeff Pinnt
المصدر: Genomics. 40(1)
مصطلحات موضوعية: MYO7A, Usher syndrome, Hearing Loss, Sensorineural, Biology, Myosins, Polymerase Chain Reaction, Exon, Gene mapping, otorhinolaryngologic diseases, Genetics, medicine, Humans, Abnormalities, Multiple, Chromosomes, Artificial, Yeast, Genomic organization, Sequence Tagged Sites, Contig, Retinal Degeneration, Dyneins, Exons, Syndrome, medicine.disease, Cosmids, Molecular biology, Introns, genomic DNA, Vestibular Diseases, Myosin VIIa, Cosmid
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7
المصدر: Human Molecular Genetics. 1:141-141
مصطلحات موضوعية: Genetics, Polymorphism, Genetic, Base Sequence, Molecular Sequence Data, Chromosome, General Medicine, Biology, Molecular biology, law.invention, Gene Frequency, Oligodeoxyribonucleotides, Gene mapping, Chromosomes, Human, Pair 1, law, Genetic marker, Humans, Repeat polymorphism, Repeated sequence, Molecular Biology, Allele frequency, Genetics (clinical), Polymerase chain reaction, Microdissection, Repetitive Sequences, Nucleic Acid
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48150eed8b9c64ba5c722ef5af82d72a
https://doi.org/10.1093/hmg/1.2.141