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Fred Gilbert

Showing results (11-20 of 16) with videos related to

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Cancer Genetics and Cytogenetics|January 28, 2003
Allelic imbalance in selected chromosomal regions in ovarian cancerLise Lotte Hansen, Lise Lind Jensen, Constantine Dimitrakakis, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
Molecular Genetics and Metabolism|July 2, 2010
Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2Lisa M Vincent, Fred Gilbert, Jennifer I DiPace, et al.
Anticancer Research|May 17, 2002
Frequent LOH at hMLH1, a highly variable SNP in hMSH3, and negligible coding instability in ovarian cancerIordanis I Arzimanoglou, Lise Lotte Hansen, David Chong, et al.
Cells|June 2, 2021
Characterization of PARP6 Function in Knockout Mice and Patients with Developmental DelayAnke Vermehren-Schmaedick, Jeffrey Y Huang, Madison Levinson, et al.
Pediatric Research|September 27, 2005
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndromeDeborah A McDermott, Michael C Bressan, Jie He, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Cancer Genetics and Cytogenetics|January 28, 2003
Allelic imbalance in selected chromosomal regions in ovarian cancerLise Lotte Hansen, Lise Lind Jensen, Constantine Dimitrakakis, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
Molecular Genetics and Metabolism|July 2, 2010
Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2Lisa M Vincent, Fred Gilbert, Jennifer I DiPace, et al.
Anticancer Research|May 17, 2002
Frequent LOH at hMLH1, a highly variable SNP in hMSH3, and negligible coding instability in ovarian cancerIordanis I Arzimanoglou, Lise Lotte Hansen, David Chong, et al.
Cells|June 2, 2021
Characterization of PARP6 Function in Knockout Mice and Patients with Developmental DelayAnke Vermehren-Schmaedick, Jeffrey Y Huang, Madison Levinson, et al.
Pediatric Research|September 27, 2005
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndromeDeborah A McDermott, Michael C Bressan, Jie He, et al.
Pageof 2