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Showing results (221-230 of 228) with videos related to

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American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
Nature Chemistry|January 3, 2025
Four-electron reduction of benzene by a samarium(II)-alkyl without the addition of external reducing agentsGeorgia M Richardson, Thayalan Rajeshkumar, Finlay M Burke, et al.
Human Molecular Genetics|February 28, 2015
Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiencyManuel Schiff, Birgit Haberberger, Chuanwu Xia, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Report of the fourth international workshop on human chromosome 15 mapping 1997C C Morton, S L Christian, T A Donlon, et al.
JCI Insight|October 15, 2020
A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editingErik A Koppes, Bethany K Redel, Marie A Johnson, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Nature|May 15, 2007
Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequencesTarjei S Mikkelsen, Matthew J Wakefield, Bronwen Aken, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
Pageof 23

Showing results (221-230 of 228) with videos related to

Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 228 results.
American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
Nature Chemistry|January 3, 2025
Four-electron reduction of benzene by a samarium(II)-alkyl without the addition of external reducing agentsGeorgia M Richardson, Thayalan Rajeshkumar, Finlay M Burke, et al.
Human Molecular Genetics|February 28, 2015
Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiencyManuel Schiff, Birgit Haberberger, Chuanwu Xia, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Report of the fourth international workshop on human chromosome 15 mapping 1997C C Morton, S L Christian, T A Donlon, et al.
JCI Insight|October 15, 2020
A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editingErik A Koppes, Bethany K Redel, Marie A Johnson, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Nature|May 15, 2007
Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequencesTarjei S Mikkelsen, Matthew J Wakefield, Bronwen Aken, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
Pageof 23