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C C Morton

Showing results (151-160 of 185) with videos related to

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Genomics|March 1, 1992
The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14L M Albritton, A M Bowcock, R L Eddy, et al.
Genomics|January 7, 1998
An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1)A B Skvorak, N G Robertson, Y Yin, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomasM Schoenberg Fejzo, H R Ashar, K S Krauter, et al.
Genomics|September 7, 2001
STK25 is a candidate gene for pseudopseudohypoparathyroidismM S Davids, E Crawford, S Weremowicz, et al.
Molecular and Cellular Biology|September 1, 1993
Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partnerP A Ney, N C Andrews, S M Jane, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
The t(10;14)(q24;q11) of T-cell acute lymphoblastic leukemia juxtaposes the delta T-cell receptor with TCL3, a conserved and activated locus at 10q24M Zutter, R D Hockett, C W Roberts, et al.
American Journal of Human Genetics|September 1, 1990
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12S D Solomon, A A Geisterfer-Lowrance, H P Vosberg, et al.
Prenatal Diagnosis|July 22, 2014
Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencingM J Macera, A Sobrino, B Levy, et al.
Journal of Medical Genetics|August 3, 2005
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1H G Kim, S R Herrick, E Lemyre, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Pageof 19

Showing results (151-160 of 185) with videos related to

Sort By:
Pageof 19
Genomics|March 1, 1992
The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14L M Albritton, A M Bowcock, R L Eddy, et al.
Genomics|January 7, 1998
An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1)A B Skvorak, N G Robertson, Y Yin, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomasM Schoenberg Fejzo, H R Ashar, K S Krauter, et al.
Genomics|September 7, 2001
STK25 is a candidate gene for pseudopseudohypoparathyroidismM S Davids, E Crawford, S Weremowicz, et al.
Molecular and Cellular Biology|September 1, 1993
Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partnerP A Ney, N C Andrews, S M Jane, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
The t(10;14)(q24;q11) of T-cell acute lymphoblastic leukemia juxtaposes the delta T-cell receptor with TCL3, a conserved and activated locus at 10q24M Zutter, R D Hockett, C W Roberts, et al.
American Journal of Human Genetics|September 1, 1990
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12S D Solomon, A A Geisterfer-Lowrance, H P Vosberg, et al.
Prenatal Diagnosis|July 22, 2014
Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencingM J Macera, A Sobrino, B Levy, et al.
Journal of Medical Genetics|August 3, 2005
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1H G Kim, S R Herrick, E Lemyre, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Pageof 19