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Laird G Jackson

Showing results (21-30 of 35) with videos related to

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Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
Human Mutation|August 25, 2009
SMC1A expression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndromeJinglan Liu, Rachel Feldman, Zhe Zhang, et al.
American Journal of Obstetrics and Gynecology|May 20, 2005
Elevated first-trimester nuchal translucency increases the risk of congenital heart defectsRay O Bahado-Singh, Ronald Wapner, Elizabeth Thom, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Germline mosaicism in Cornelia de Lange syndromeThomas P Slavin, Noam Lazebnik, Dinah M Clark, et al.
Plos Biology|May 27, 2009
Transcriptional dysregulation in NIPBL and cohesin mutant human cellsJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Lancet (London, England)|January 18, 2003
Intact fetal cells in maternal plasma: are they really there?Farideh Z Bischoff, Sinuhe Hahn, Kirby L Johnson, et al.
Nucleic Acids Research|May 8, 2010
Genome-wide DNA methylation analysis in cohesin mutant human cell linesJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Obstetrics and Gynecology|March 2, 2005
Late first-trimester placental disruption and subsequent gestational hypertension/preeclampsiaRichard K Silver, R Douglas Wilson, John Philip, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and GenomicsFrederick R Bieber, Athena M Cherry, Beverly S Emanuel, et al.
Nature Genetics|May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BIan D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
Human Mutation|August 25, 2009
SMC1A expression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndromeJinglan Liu, Rachel Feldman, Zhe Zhang, et al.
American Journal of Obstetrics and Gynecology|May 20, 2005
Elevated first-trimester nuchal translucency increases the risk of congenital heart defectsRay O Bahado-Singh, Ronald Wapner, Elizabeth Thom, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Germline mosaicism in Cornelia de Lange syndromeThomas P Slavin, Noam Lazebnik, Dinah M Clark, et al.
Plos Biology|May 27, 2009
Transcriptional dysregulation in NIPBL and cohesin mutant human cellsJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Lancet (London, England)|January 18, 2003
Intact fetal cells in maternal plasma: are they really there?Farideh Z Bischoff, Sinuhe Hahn, Kirby L Johnson, et al.
Nucleic Acids Research|May 8, 2010
Genome-wide DNA methylation analysis in cohesin mutant human cell linesJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Obstetrics and Gynecology|March 2, 2005
Late first-trimester placental disruption and subsequent gestational hypertension/preeclampsiaRichard K Silver, R Douglas Wilson, John Philip, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and GenomicsFrederick R Bieber, Athena M Cherry, Beverly S Emanuel, et al.
Nature Genetics|May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BIan D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
Pageof 4