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Mark D Pertile

Showing results (1-10 of 37) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|May 30, 2014
Chromosome microarrays in diagnostic testing: interpreting the genomic dataGreg B Peters, Mark D Pertile
Methods in Molecular Biology (Clifton, N.J.)|December 3, 2017
Isolation and Characterization of Mesenchymal Stem/Stromal Cells Derived from Human Third Trimester Placental Chorionic Villi and Decidua BasalisGina D Kusuma, Mohamed H Abumaree, Mark D Pertile, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Questionable pathogenicity of FOXG1 duplicationDavid J Amor, Trent Burgess, Tiong Y Tan, et al.
Genome Research|September 10, 2009
Rapid evolution of mouse Y centromere repeat DNA belies recent sequence stabilityMark D Pertile, Alison N Graham, K H Andy Choo, et al.
Prenatal Diagnosis|July 8, 2015
Maternal mosaicism for a large segmental duplication of 18q as a secondary finding following non-invasive prenatal testing and implications for test accuracyNicola Flowers, Joanne Kelley, Styrmir Sigurjonsson, et al.
The Journal of Pediatrics|September 3, 2004
Monozygotic twins with discordant karyotypes: a case reportColm P F O'Donnell, Mark D Pertile, Leslie J Sheffield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 7, 2019
The clinical benefit of genome-wide cfDNA testing cannot be extrapolated from CVS dataErik A Sistermans, Diane Van Opstal, Mireille N Bekker, et al.
BMC Medicine|August 26, 2016
Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screeningPaul A Cohen, Nicola Flowers, Stephen Tong, et al.
Case Reports in Genetics|March 21, 2014
Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureTrent Burgess, Lilian Downie, Mark D Pertile, et al.
BMC Pregnancy and Childbirth|May 14, 2024
Disparities in integrating non-invasive prenatal testing into antenatal healthcare in Australia: a survey of healthcare professionalsMolly Johnston, Lisa Hui, Hilary Bowman-Smart, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Methods in Molecular Biology (Clifton, N.J.)|May 30, 2014
Chromosome microarrays in diagnostic testing: interpreting the genomic dataGreg B Peters, Mark D Pertile
Methods in Molecular Biology (Clifton, N.J.)|December 3, 2017
Isolation and Characterization of Mesenchymal Stem/Stromal Cells Derived from Human Third Trimester Placental Chorionic Villi and Decidua BasalisGina D Kusuma, Mohamed H Abumaree, Mark D Pertile, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Questionable pathogenicity of FOXG1 duplicationDavid J Amor, Trent Burgess, Tiong Y Tan, et al.
Genome Research|September 10, 2009
Rapid evolution of mouse Y centromere repeat DNA belies recent sequence stabilityMark D Pertile, Alison N Graham, K H Andy Choo, et al.
Prenatal Diagnosis|July 8, 2015
Maternal mosaicism for a large segmental duplication of 18q as a secondary finding following non-invasive prenatal testing and implications for test accuracyNicola Flowers, Joanne Kelley, Styrmir Sigurjonsson, et al.
The Journal of Pediatrics|September 3, 2004
Monozygotic twins with discordant karyotypes: a case reportColm P F O'Donnell, Mark D Pertile, Leslie J Sheffield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 7, 2019
The clinical benefit of genome-wide cfDNA testing cannot be extrapolated from CVS dataErik A Sistermans, Diane Van Opstal, Mireille N Bekker, et al.
BMC Medicine|August 26, 2016
Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screeningPaul A Cohen, Nicola Flowers, Stephen Tong, et al.
Case Reports in Genetics|March 21, 2014
Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureTrent Burgess, Lilian Downie, Mark D Pertile, et al.
BMC Pregnancy and Childbirth|May 14, 2024
Disparities in integrating non-invasive prenatal testing into antenatal healthcare in Australia: a survey of healthcare professionalsMolly Johnston, Lisa Hui, Hilary Bowman-Smart, et al.
Pageof 4