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C Brody

Showing results (211-220 of 234) with videos related to

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American Journal of Human Genetics|May 3, 2016
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of CobalaminAnne M Molloy, Faith Pangilinan, James L Mills, et al.
Genomics|October 15, 1996
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1K J Abel, L C Brody, J M Valdes, et al.
European Journal of Human Genetics : EJHG|January 17, 2021
The genetic landscape of polycystic kidney disease in IrelandKatherine A Benson, Susan L Murray, Sarah R Senum, et al.
BMC Medical Genetics|August 4, 2012
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defectsFaith Pangilinan, Anne M Molloy, James L Mills, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 childrenGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Nature Genetics|September 10, 1998
The APCI1307K allele and breast cancer riskM Redston, K L Nathanson, Z Q Yuan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 26, 2012
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide associationKarl C Desch, Ayse B Ozel, David Siemieniak, et al.
American Journal of Medical Genetics. Part A|June 18, 2022
Exome sequencing identifies genetic variants in anophthalmia and microphthalmiaJingjing Li, Wei Yang, Yuejun Jessie Wang, et al.
Nature Genetics|March 31, 2009
Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanomaLavanya H Palavalli, Todd D Prickett, John R Wunderlich, et al.
Birth Defects Research|July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyElizabeth E Blue, Kristin J Moore, Kari E North, et al.
Pageof 24

Showing results (211-220 of 234) with videos related to

Sort By:
Pageof 24
American Journal of Human Genetics|May 3, 2016
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of CobalaminAnne M Molloy, Faith Pangilinan, James L Mills, et al.
Genomics|October 15, 1996
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1K J Abel, L C Brody, J M Valdes, et al.
European Journal of Human Genetics : EJHG|January 17, 2021
The genetic landscape of polycystic kidney disease in IrelandKatherine A Benson, Susan L Murray, Sarah R Senum, et al.
BMC Medical Genetics|August 4, 2012
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defectsFaith Pangilinan, Anne M Molloy, James L Mills, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 childrenGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Nature Genetics|September 10, 1998
The APCI1307K allele and breast cancer riskM Redston, K L Nathanson, Z Q Yuan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 26, 2012
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide associationKarl C Desch, Ayse B Ozel, David Siemieniak, et al.
American Journal of Medical Genetics. Part A|June 18, 2022
Exome sequencing identifies genetic variants in anophthalmia and microphthalmiaJingjing Li, Wei Yang, Yuejun Jessie Wang, et al.
Nature Genetics|March 31, 2009
Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanomaLavanya H Palavalli, Todd D Prickett, John R Wunderlich, et al.
Birth Defects Research|July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyElizabeth E Blue, Kristin J Moore, Kari E North, et al.
Pageof 24