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Howard R Slater

Showing results (11-20 of 43) with videos related to

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American Journal of Medical Genetics. Part A|May 20, 2015
Prenatal diagnosis of fragile X syndrome complicated by full mutation retractionZornitza Stark, David Francis, Lydia Gaffney, et al.
Prenatal Diagnosis|April 29, 2008
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversionK Prabhakara, Damien L Bruno, Priya Padman, et al.
BMC Medical Genetics|May 10, 2005
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeBirgitt Schüle, Mohammed Albalwi, Emma Northrop, et al.
Plos One|February 4, 2014
Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discoveryDineika Chandrananda, Natalie P Thorne, Devika Ganesamoorthy, et al.
BMC Clinical Pathology|June 10, 2009
Improved methodology for assessment of mRNA levels in blood of patients with FMR1 related disordersDavid E Godler, Danuta Z Loesch, Richard Huggins, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 13, 2018
Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunctionJohn B Whitlam, Ling Ling, Alison Skene, et al.
Human Genetics|February 16, 2005
Molecular distinction between true centric fission and pericentric duplication-fissionJo Perry, Sara Nouri, Phung La, et al.
American Journal of Human Genetics|October 28, 2005
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPsHoward R Slater, Dione K Bailey, Hua Ren, et al.
American Journal of Human Genetics|March 15, 2006
Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic VariationsHoward R Slater, Dione K Bailey, Hua Ren, et al.
Human Mutation|September 20, 2005
Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assayEmma L Northrop, Hua Ren, Damien L Bruno, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|May 20, 2015
Prenatal diagnosis of fragile X syndrome complicated by full mutation retractionZornitza Stark, David Francis, Lydia Gaffney, et al.
Prenatal Diagnosis|April 29, 2008
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversionK Prabhakara, Damien L Bruno, Priya Padman, et al.
BMC Medical Genetics|May 10, 2005
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeBirgitt Schüle, Mohammed Albalwi, Emma Northrop, et al.
Plos One|February 4, 2014
Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discoveryDineika Chandrananda, Natalie P Thorne, Devika Ganesamoorthy, et al.
BMC Clinical Pathology|June 10, 2009
Improved methodology for assessment of mRNA levels in blood of patients with FMR1 related disordersDavid E Godler, Danuta Z Loesch, Richard Huggins, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 13, 2018
Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunctionJohn B Whitlam, Ling Ling, Alison Skene, et al.
Human Genetics|February 16, 2005
Molecular distinction between true centric fission and pericentric duplication-fissionJo Perry, Sara Nouri, Phung La, et al.
American Journal of Human Genetics|October 28, 2005
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPsHoward R Slater, Dione K Bailey, Hua Ren, et al.
American Journal of Human Genetics|March 15, 2006
Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic VariationsHoward R Slater, Dione K Bailey, Hua Ren, et al.
Human Mutation|September 20, 2005
Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assayEmma L Northrop, Hua Ren, Damien L Bruno, et al.
Pageof 5