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Kristen Sund

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Human Molecular Genetics|October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephalyAndrew DiStasio, Ashley Driver, Kristen Sund, et al.
Molecular Genetics & Genomic Medicine|September 8, 2019
Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic featuresBianca E Russell, Diana Rigueur, Kathryn N Weaver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephalyAndrew DiStasio, Ashley Driver, Kristen Sund, et al.
Molecular Genetics & Genomic Medicine|September 8, 2019
Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic featuresBianca E Russell, Diana Rigueur, Kathryn N Weaver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 1