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Lisa G Shaffer

Showing results (71-80 of 215) with videos related to

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American Journal of Medical Genetics. Part A|October 30, 2008
Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)Marzena Gajecka, Reem Saadeh, Katherine L Mackay, et al.
Prenatal Diagnosis|October 7, 2010
Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal settingIdit Maya, Bella Davidov, Liron Gershovitz, et al.
Methods in Molecular Medicine|October 31, 2006
Comparative genomic hybridization by microarray for the detection of cytogenetic imbalanceMalgorzata Jarmuz, Blake C Ballif, Catherine D Kashork, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Mosaicism in a patient with Down syndrome reveals post-fertilization formation of a Robertsonian translocation and isochromosomeRuma Bandyopadhyay, Christopher McCaskill, Cami Knox-Du Bois, et al.
Prenatal Diagnosis|February 24, 2006
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridizationBlake C Ballif, Catherine D Kashork, Reza Saleki, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|December 7, 2005
Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32Alberto L Rosa, Yuan-Qing Wu, Bernard Kwabi-Addo, et al.
American Journal of Human Genetics|November 9, 2002
Parental origin and timing of de novo Robertsonian translocation formationRuma Bandyopadhyay, Anita Heller, Cami Knox-DuBois, et al.
Human Genetics|April 10, 2002
Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontiaParimal Das, David W Stockton, Christopher Bauer, et al.
Acta Neuropathologica Communications|November 21, 2013
Neuropathology of brain and spinal malformations in a case of monosomy 1p36Naoko Shiba, Ray A M Daza, Lisa G Shaffer, et al.
The Journal of Pediatrics|July 25, 2006
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical casesLisa G Shaffer, Catherine D Kashork, Reza Saleki, et al.
Pageof 22

Showing results (71-80 of 215) with videos related to

Sort By:
Pageof 22
American Journal of Medical Genetics. Part A|October 30, 2008
Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)Marzena Gajecka, Reem Saadeh, Katherine L Mackay, et al.
Prenatal Diagnosis|October 7, 2010
Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal settingIdit Maya, Bella Davidov, Liron Gershovitz, et al.
Methods in Molecular Medicine|October 31, 2006
Comparative genomic hybridization by microarray for the detection of cytogenetic imbalanceMalgorzata Jarmuz, Blake C Ballif, Catherine D Kashork, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Mosaicism in a patient with Down syndrome reveals post-fertilization formation of a Robertsonian translocation and isochromosomeRuma Bandyopadhyay, Christopher McCaskill, Cami Knox-Du Bois, et al.
Prenatal Diagnosis|February 24, 2006
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridizationBlake C Ballif, Catherine D Kashork, Reza Saleki, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|December 7, 2005
Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32Alberto L Rosa, Yuan-Qing Wu, Bernard Kwabi-Addo, et al.
American Journal of Human Genetics|November 9, 2002
Parental origin and timing of de novo Robertsonian translocation formationRuma Bandyopadhyay, Anita Heller, Cami Knox-DuBois, et al.
Human Genetics|April 10, 2002
Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontiaParimal Das, David W Stockton, Christopher Bauer, et al.
Acta Neuropathologica Communications|November 21, 2013
Neuropathology of brain and spinal malformations in a case of monosomy 1p36Naoko Shiba, Ray A M Daza, Lisa G Shaffer, et al.
The Journal of Pediatrics|July 25, 2006
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical casesLisa G Shaffer, Catherine D Kashork, Reza Saleki, et al.
Pageof 22