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Showing results (201-210 of 210) with videos related to

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American Journal of Human Genetics|October 18, 2000
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait lociR M Watanabe, S Ghosh, C D Langefeld, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Scientific Reports|July 21, 2021
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
Scientific Reports|October 23, 2020
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
American Journal of Human Genetics|June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft TriosMadison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.
American Journal of Human Genetics|September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Nature|August 13, 2013
De novo mutations in epileptic encephalopathies, , Andrew S Allen, et al.
Nature Medicine|August 7, 2023
Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer's diseaseErik C B Johnson, Shijia Bian, Rafi U Haque, et al.
Diabetes|February 28, 2004
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14Kaisa Silander, Laura J Scott, Timo T Valle, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 21

Showing results (201-210 of 210) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 210 results.
American Journal of Human Genetics|October 18, 2000
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait lociR M Watanabe, S Ghosh, C D Langefeld, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Scientific Reports|July 21, 2021
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
Scientific Reports|October 23, 2020
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
American Journal of Human Genetics|June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft TriosMadison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.
American Journal of Human Genetics|September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Nature|August 13, 2013
De novo mutations in epileptic encephalopathies, , Andrew S Allen, et al.
Nature Medicine|August 7, 2023
Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer's diseaseErik C B Johnson, Shijia Bian, Rafi U Haque, et al.
Diabetes|February 28, 2004
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14Kaisa Silander, Laura J Scott, Timo T Valle, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 21