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Plos Genetics
|
March 22, 2014
Modeling 3D facial shape from DNA
Peter Claes, Denise K Liberton, Katleen Daniels, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 27, 2020
A state-based approach to genomics for rare disease and population screening
Kelly M East, Whitley V Kelley, Ashley Cannon, et al.
Science (New York, N.Y.)
|
September 22, 2012
Specifying and sustaining pigmentation patterns in domestic and wild cats
Christopher B Kaelin, Xiao Xu, Lewis Z Hong, et al.
American Journal of Human Genetics
|
December 12, 2018
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies
Gemma L Carvill, Krysta L Engel, Aishwarya Ramamurthy, et al.
Genome Medicine
|
May 31, 2017
Genomic diagnosis for children with intellectual disability and/or developmental delay
Kevin M Bowling, Michelle L Thompson, Michelle D Amaral, et al.
Plos Genetics
|
December 1, 2018
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
Susan M Hiatt, Matthew B Neu, Ryne C Ramaker, et al.
Current Biology : CB
|
December 17, 2022
Genetic architecture and evolution of color variation in American black bears
Emily E Puckett, Isis S Davis, Dawn C Harper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 21, 2021
Genome sequencing as a first-line diagnostic test for hospitalized infants
Kevin M Bowling, Michelle L Thompson, Candice R Finnila, et al.
Journal of Personalized Medicine
|
July 29, 2023
Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
Amy A Lemke, Michelle L Thompson, Emily C Gimpel, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 139) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 139 results.
Plos Genetics
|
March 22, 2014
Modeling 3D facial shape from DNA
Peter Claes, Denise K Liberton, Katleen Daniels, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 27, 2020
A state-based approach to genomics for rare disease and population screening
Kelly M East, Whitley V Kelley, Ashley Cannon, et al.
Science (New York, N.Y.)
|
September 22, 2012
Specifying and sustaining pigmentation patterns in domestic and wild cats
Christopher B Kaelin, Xiao Xu, Lewis Z Hong, et al.
American Journal of Human Genetics
|
December 12, 2018
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies
Gemma L Carvill, Krysta L Engel, Aishwarya Ramamurthy, et al.
Genome Medicine
|
May 31, 2017
Genomic diagnosis for children with intellectual disability and/or developmental delay
Kevin M Bowling, Michelle L Thompson, Michelle D Amaral, et al.
Plos Genetics
|
December 1, 2018
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
Susan M Hiatt, Matthew B Neu, Ryne C Ramaker, et al.
Current Biology : CB
|
December 17, 2022
Genetic architecture and evolution of color variation in American black bears
Emily E Puckett, Isis S Davis, Dawn C Harper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 21, 2021
Genome sequencing as a first-line diagnostic test for hospitalized infants
Kevin M Bowling, Michelle L Thompson, Candice R Finnila, et al.
Journal of Personalized Medicine
|
July 29, 2023
Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
Amy A Lemke, Michelle L Thompson, Emily C Gimpel, et al.
Page
of 14