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H Hensel

Showing results (71-80 of 84) with videos related to

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International Journal of Molecular Sciences|December 13, 2016
Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersKaren S Ho, E Robert Wassman, Adrianne L Baxter, et al.
Biomed Research International|December 16, 2016
Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersKaren S Ho, Hope Twede, Rena Vanzo, et al.
Virchows Archiv : an International Journal of Pathology|January 1, 1994
p53 mutations in gastric and colorectal cancers in Texas Hispanics versus AnglosB G Schneider, S G Hilsenbeck, C H Hensel, et al.
Genomics|February 15, 1996
Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancerR H Xiang, C H Hensel, D K Garcia, et al.
Journal of Medical Genetics|January 10, 2016
Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndromeKaren S Ho, Sarah T South, Amanda Lortz, et al.
Scientific Reports|October 27, 2019
Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X TestingCharles H Hensel, Rena J Vanzo, Megan M Martin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2005
Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disordersNicola J Camp, Michael R Lowry, R Lynn Richards, et al.
Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Plos One|January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD populationNori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Oncogene|December 5, 1996
An 80 Kb P1 clone from chromosome 3p21.3 suppresses tumor growth in vivoM C Todd, R H Xiang, D K Garcia, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
International Journal of Molecular Sciences|December 13, 2016
Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersKaren S Ho, E Robert Wassman, Adrianne L Baxter, et al.
Biomed Research International|December 16, 2016
Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersKaren S Ho, Hope Twede, Rena Vanzo, et al.
Virchows Archiv : an International Journal of Pathology|January 1, 1994
p53 mutations in gastric and colorectal cancers in Texas Hispanics versus AnglosB G Schneider, S G Hilsenbeck, C H Hensel, et al.
Genomics|February 15, 1996
Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancerR H Xiang, C H Hensel, D K Garcia, et al.
Journal of Medical Genetics|January 10, 2016
Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndromeKaren S Ho, Sarah T South, Amanda Lortz, et al.
Scientific Reports|October 27, 2019
Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X TestingCharles H Hensel, Rena J Vanzo, Megan M Martin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2005
Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disordersNicola J Camp, Michael R Lowry, R Lynn Richards, et al.
Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Plos One|January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD populationNori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Oncogene|December 5, 1996
An 80 Kb P1 clone from chromosome 3p21.3 suppresses tumor growth in vivoM C Todd, R H Xiang, D K Garcia, et al.
Pageof 9