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Elizabeth W McPherson

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American Journal of Medical Genetics. Part A|February 26, 2021
3137 fetuses in 33 years: What we have learned from the Wisconsin stillbirth service programElizabeth W McPherson
Journal of Genetic Counseling|May 25, 2010
Patient and family experiences and opinions on adding 22q11 deletion syndrome to the newborn screenAbigail M Bales, Christina A Zaleski, Elizabeth W McPherson
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2010
Newborn screening programs: should 22q11 deletion syndrome be added?Abigail M Bales, Christina A Zaleski, Elizabeth W McPherson
American Journal of Medical Genetics. Part A|March 21, 2013
Intestinal ganglioneuromatosis: unusual presentation of Cowden syndrome resulting in delayed diagnosisAnna Vinitsky, Christina A Zaleski, Sayed M Sajjad, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 23, 2009
Janiceps conjoined twins with extreme asymmetry: case report with complete autopsy and histopathologic findingsHannah A Kastenbaum, Elizabeth W McPherson, Geoffrey H Murdoch, et al.
Prenatal Diagnosis|March 25, 2006
Variable outcomes in mosaic trisomy 16: five case reports and literature analysisKatherine Neiswanger, Paul M Hohler, Lori B Hively-Thomas, et al.
Plos One|December 9, 2016
Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health RecordsKaren Y He, Yiqing Zhao, Elizabeth W McPherson, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.
Journal of Medical Genetics|January 15, 2015
SeqHBase: a big data toolset for family based sequencing data analysisMin He, Thomas N Person, Scott J Hebbring, et al.
American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|February 26, 2021
3137 fetuses in 33 years: What we have learned from the Wisconsin stillbirth service programElizabeth W McPherson
Journal of Genetic Counseling|May 25, 2010
Patient and family experiences and opinions on adding 22q11 deletion syndrome to the newborn screenAbigail M Bales, Christina A Zaleski, Elizabeth W McPherson
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2010
Newborn screening programs: should 22q11 deletion syndrome be added?Abigail M Bales, Christina A Zaleski, Elizabeth W McPherson
American Journal of Medical Genetics. Part A|March 21, 2013
Intestinal ganglioneuromatosis: unusual presentation of Cowden syndrome resulting in delayed diagnosisAnna Vinitsky, Christina A Zaleski, Sayed M Sajjad, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 23, 2009
Janiceps conjoined twins with extreme asymmetry: case report with complete autopsy and histopathologic findingsHannah A Kastenbaum, Elizabeth W McPherson, Geoffrey H Murdoch, et al.
Prenatal Diagnosis|March 25, 2006
Variable outcomes in mosaic trisomy 16: five case reports and literature analysisKatherine Neiswanger, Paul M Hohler, Lori B Hively-Thomas, et al.
Plos One|December 9, 2016
Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health RecordsKaren Y He, Yiqing Zhao, Elizabeth W McPherson, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.
Journal of Medical Genetics|January 15, 2015
SeqHBase: a big data toolset for family based sequencing data analysisMin He, Thomas N Person, Scott J Hebbring, et al.
American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.
Pageof 2