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David W Craig

Showing results (41-50 of 161) with videos related to

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Human Molecular Genetics|May 14, 2013
In vitro-differentiated neural cell cultures progress towards donor-identical brain tissueBrooke E Hjelm, Bodour Salhia, Ahmet Kurdoglu, et al.
American Journal of Human Genetics|February 7, 2008
Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locusDavid W Craig, Abraham Itty, Corrie Panganiban, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite populationKevin A Strauss, Erik G Puffenberger, David W Craig, et al.
Molecular Genetics & Genomic Medicine|January 7, 2022
Progressive cerebellar atrophy caused by heterozygous TECPR2 mutationsKeri Ramsey, Newell Belnap, Anna Bonfitto, et al.
Cancer Research|October 25, 2022
Spatial Transcriptomic Analysis of a Diverse Patient Cohort Reveals a Conserved Architecture in Triple-Negative Breast CancerRania Bassiouni, Michael O Idowu, Lee D Gibbs, et al.
The Journal of Arthroplasty|June 11, 2025
Whole Exome Sequencing of Total Joint Arthroplasty Patients Who Have Known Venous Thromboembolism: A Pilot StudyCory K Mayfield, Elizabeth Lechtholz-Zey, Mina Ayad, et al.
Nucleic Acids Research|September 28, 2013
Long insert whole genome sequencing for copy number variant and translocation detectionWinnie S Liang, Jessica Aldrich, Waibhav Tembe, et al.
BMC Genomics|October 4, 2005
Identification of disease causing loci using an array-based genotyping approach on pooled DNADavid W Craig, Matthew J Huentelman, Diane Hu-Lince, et al.
Human Mutation|October 30, 2019
Utilizing RNA and outlier analysis to identify an intronic splice-altering variant in AP4S1 in a sibling pair with progressive spastic paraplegiaCarmel G McCullough, Szabolcs Szelinger, Newell Belnap, et al.
Neurobiology of Aging|December 3, 2014
Alzheimer's disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytesShobana Sekar, Jacquelyn McDonald, Lori Cuyugan, et al.
Pageof 17

Showing results (41-50 of 161) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|May 14, 2013
In vitro-differentiated neural cell cultures progress towards donor-identical brain tissueBrooke E Hjelm, Bodour Salhia, Ahmet Kurdoglu, et al.
American Journal of Human Genetics|February 7, 2008
Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locusDavid W Craig, Abraham Itty, Corrie Panganiban, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite populationKevin A Strauss, Erik G Puffenberger, David W Craig, et al.
Molecular Genetics & Genomic Medicine|January 7, 2022
Progressive cerebellar atrophy caused by heterozygous TECPR2 mutationsKeri Ramsey, Newell Belnap, Anna Bonfitto, et al.
Cancer Research|October 25, 2022
Spatial Transcriptomic Analysis of a Diverse Patient Cohort Reveals a Conserved Architecture in Triple-Negative Breast CancerRania Bassiouni, Michael O Idowu, Lee D Gibbs, et al.
The Journal of Arthroplasty|June 11, 2025
Whole Exome Sequencing of Total Joint Arthroplasty Patients Who Have Known Venous Thromboembolism: A Pilot StudyCory K Mayfield, Elizabeth Lechtholz-Zey, Mina Ayad, et al.
Nucleic Acids Research|September 28, 2013
Long insert whole genome sequencing for copy number variant and translocation detectionWinnie S Liang, Jessica Aldrich, Waibhav Tembe, et al.
BMC Genomics|October 4, 2005
Identification of disease causing loci using an array-based genotyping approach on pooled DNADavid W Craig, Matthew J Huentelman, Diane Hu-Lince, et al.
Human Mutation|October 30, 2019
Utilizing RNA and outlier analysis to identify an intronic splice-altering variant in AP4S1 in a sibling pair with progressive spastic paraplegiaCarmel G McCullough, Szabolcs Szelinger, Newell Belnap, et al.
Neurobiology of Aging|December 3, 2014
Alzheimer's disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytesShobana Sekar, Jacquelyn McDonald, Lori Cuyugan, et al.
Pageof 17