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C C Morton

Showing results (11-20 of 185) with videos related to

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Human Reproduction Update|February 24, 2001
Leiomyomata: heritability and cytogenetic studiesA H Ligon, C C Morton
Clinical Genetics|May 20, 1999
Beginning of a molecular era in hearing and deafnessN G Robertson, C C Morton
Genomics|June 1, 1992
Mapping and characterization of a novel human myc-like (MYCLK1) sequenceN G Robertson, C C Morton
Human Genetics|January 1, 1985
Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridizationT P Dryja, C C Morton
Genes, Chromosomes & Cancer|June 22, 2000
Genetics of uterine leiomyomataA H Ligon, C C Morton
Current Opinion in Pediatrics|December 11, 1999
Genetic causes of nonsyndromic hearing lossA B Skvorak Giersch, C C Morton
Bulletin Du Cancer|December 10, 1999
[Genetics of uterine leiomyomata]F Pedeutour, A H Ligon, C C Morton
Hearing 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 Morton
Genomics|August 1, 1994
Localization of serum biotinidase (BTD) to human chromosome 3 in band p25H Cole, S Weremowicz, C C Morton, 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 Morton
Pageof 19

Showing results (11-20 of 185) with videos related to

Sort By:
Pageof 19
Human Reproduction Update|February 24, 2001
Leiomyomata: heritability and cytogenetic studiesA H Ligon, C C Morton
Clinical Genetics|May 20, 1999
Beginning of a molecular era in hearing and deafnessN G Robertson, C C Morton
Genomics|June 1, 1992
Mapping and characterization of a novel human myc-like (MYCLK1) sequenceN G Robertson, C C Morton
Human Genetics|January 1, 1985
Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridizationT P Dryja, C C Morton
Genes, Chromosomes & Cancer|June 22, 2000
Genetics of uterine leiomyomataA H Ligon, C C Morton
Current Opinion in Pediatrics|December 11, 1999
Genetic causes of nonsyndromic hearing lossA B Skvorak Giersch, C C Morton
Bulletin Du Cancer|December 10, 1999
[Genetics of uterine leiomyomata]F Pedeutour, A H Ligon, C C Morton
Hearing 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 Morton
Genomics|August 1, 1994
Localization of serum biotinidase (BTD) to human chromosome 3 in band p25H Cole, S Weremowicz, C C Morton, 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 Morton
Pageof 19