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Mark D Pertile

Showing results (31-40 of 37) with videos related to

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JCO Precision Oncology|January 7, 2022
Cancer Diagnoses Following Abnormal Noninvasive Prenatal Testing: A Case Series, Literature Review, and Proposed Management ModelEryn Dow, Alison Freimund, Kortnye Smith, et al.
European Journal of Human Genetics : EJHG|June 15, 2018
Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndromeKarin Huijsdens-van Amsterdam, Lieve Page-Christiaens, Nicola Flowers, et al.
Scientific Reports|July 28, 2016
Haplotyping the human leukocyte antigen system from single chromosomesNicholas M Murphy, Matthew Burton, David R Powell, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Unstable Robertsonian translocations der(13;15)(q10;q10): heritable chromosome fission without phenotypic effect in two kindredsJo Perry, Sue M White, Sara Nouri, et al.
Human Reproduction (Oxford, England)|March 25, 2020
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohortLisa Hui, Alice Poulton, Eliza Kluckow, et al.
Prenatal Diagnosis|November 7, 2019
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016Eliza Kluckow, Jane Halliday, Alice Poulton, et al.
American Journal of Obstetrics and Gynecology|May 6, 2021
Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage studyLisa Hui, Cecilia Pynaker, Leonard Bonacquisto, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
JCO Precision Oncology|January 7, 2022
Cancer Diagnoses Following Abnormal Noninvasive Prenatal Testing: A Case Series, Literature Review, and Proposed Management ModelEryn Dow, Alison Freimund, Kortnye Smith, et al.
European Journal of Human Genetics : EJHG|June 15, 2018
Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndromeKarin Huijsdens-van Amsterdam, Lieve Page-Christiaens, Nicola Flowers, et al.
Scientific Reports|July 28, 2016
Haplotyping the human leukocyte antigen system from single chromosomesNicholas M Murphy, Matthew Burton, David R Powell, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Unstable Robertsonian translocations der(13;15)(q10;q10): heritable chromosome fission without phenotypic effect in two kindredsJo Perry, Sue M White, Sara Nouri, et al.
Human Reproduction (Oxford, England)|March 25, 2020
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohortLisa Hui, Alice Poulton, Eliza Kluckow, et al.
Prenatal Diagnosis|November 7, 2019
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016Eliza Kluckow, Jane Halliday, Alice Poulton, et al.
American Journal of Obstetrics and Gynecology|May 6, 2021
Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage studyLisa Hui, Cecilia Pynaker, Leonard Bonacquisto, et al.
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