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Archives of Otolaryngology--Head & Neck Surgery|December 1, 1993
COL1A2 and COL2A1 expression in temporal bone of lethal osteogenesis imperfectaU Khetarpal, C C MortonGenetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
A new age in the genetics of deafnessH L Rehm, C C MortonGenomics|June 1, 1992
Mapping and characterization of a novel human myc-like (MYCLK1) sequenceN G Robertson, C C MortonHuman Genetics|January 1, 1985
Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridizationT P Dryja, C C MortonEuropean Journal of Human Genetics : EJHG|June 15, 2000
Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approachA H Ligon, C D Kashork, C S Richards, et al.Cytogenetic and Genome Research|December 28, 2007
Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3)J C Hodge, A Lawson-Yuen, J M Stoler, et al.Current Opinion in Pediatrics|December 11, 1999
Genetic causes of nonsyndromic hearing lossA B Skvorak Giersch, C C MortonHearing Research|September 15, 1996
Detection of cone alpha transducin mRNA in human fetal cochlea: negative mutation analysis in Usher syndromeI Magovcevic, E L Berson, C C MortonGenes, Chromosomes & Cancer|April 1, 1995
Two tumor suppressive loci on chromosome 10 involved in human glioblastomasP A Steck, A H Ligon, P Cheong, et al.Cancer Genetics and Cytogenetics|October 6, 1997
The del(7q) subgroup in uterine leiomyomata: genetic and biologic characteristics. Further evidence for the secondary nature of cytogenetic abnormalities in the pathobiology of uterine leiomyomataY P Xing, W L Powell, C C MortonPageof 18