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Alison E Gardner

Showing results (1-10 of 19) with videos related to

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Oncology (Williston Park, N.Y.)|August 9, 2012
Eat your vegetablesAlison E Gardner
Molecular Cancer|August 11, 2004
Aberrant CBFA2T3B gene promoter methylation in breast tumorsAnthony J Bais, Alison E Gardner, Olivia L D McKenzie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 23, 2024
Application of multiple mosaic callers improves post-zygotic mutation detection from exome sequencing dataNandini G Sandran, Dani L Fornarino, Mark A Corbett, et al.
Journal of Human Genetics|May 19, 2004
The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 geneKavita Bhalla, Hilary A Phillips, Joanna Crawford, et al.
Genomics|September 6, 2002
Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genesJason A Powell, Alison E Gardner, Anthony J Bais, et al.
American Journal of Human Genetics|August 28, 2010
A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Mark A Corbett, Melanie Bahlo, Lachlan Jolly, et al.
NPJ Genomic Medicine|December 20, 2018
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
NPJ Genomic Medicine|June 25, 2019
Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
Cancer Research|August 17, 2002
CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3Marina Kochetkova, Olivia L D McKenzie, Anthony J Bais, et al.
American Journal of Human Genetics|May 10, 2011
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaMark A Corbett, Michael Schwake, Melanie Bahlo, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Oncology (Williston Park, N.Y.)|August 9, 2012
Eat your vegetablesAlison E Gardner
Molecular Cancer|August 11, 2004
Aberrant CBFA2T3B gene promoter methylation in breast tumorsAnthony J Bais, Alison E Gardner, Olivia L D McKenzie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 23, 2024
Application of multiple mosaic callers improves post-zygotic mutation detection from exome sequencing dataNandini G Sandran, Dani L Fornarino, Mark A Corbett, et al.
Journal of Human Genetics|May 19, 2004
The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 geneKavita Bhalla, Hilary A Phillips, Joanna Crawford, et al.
Genomics|September 6, 2002
Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genesJason A Powell, Alison E Gardner, Anthony J Bais, et al.
American Journal of Human Genetics|August 28, 2010
A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Mark A Corbett, Melanie Bahlo, Lachlan Jolly, et al.
NPJ Genomic Medicine|December 20, 2018
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
NPJ Genomic Medicine|June 25, 2019
Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
Cancer Research|August 17, 2002
CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3Marina Kochetkova, Olivia L D McKenzie, Anthony J Bais, et al.
American Journal of Human Genetics|May 10, 2011
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaMark A Corbett, Michael Schwake, Melanie Bahlo, et al.
Pageof 2