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B Crowley

Showing results (171-180 of 174) with videos related to

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Human Molecular Genetics|January 24, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Tingwei Guo, Alexander Diacou, Hiroko Nomaru, et al.
American Journal of Human Genetics|August 28, 2020
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS ProjectTamara S Roman, Stephanie B Crowley, Myra I Roche, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjectsYingjie Zhao, Tingwei Guo, Ania Fiksinski, et al.
The New England Journal of Medicine|January 26, 2017
Genetic Drivers of Kidney Defects in the DiGeorge SyndromeEsther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, et al.
Pageof 18

Showing results (171-180 of 174) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 174 results.
Human Molecular Genetics|January 24, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Tingwei Guo, Alexander Diacou, Hiroko Nomaru, et al.
American Journal of Human Genetics|August 28, 2020
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS ProjectTamara S Roman, Stephanie B Crowley, Myra I Roche, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjectsYingjie Zhao, Tingwei Guo, Ania Fiksinski, et al.
The New England Journal of Medicine|January 26, 2017
Genetic Drivers of Kidney Defects in the DiGeorge SyndromeEsther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, et al.
Pageof 18