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Showing results (141-150 of 146) with videos related to

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Human Molecular Genetics|May 1, 1997
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?B S Andresen, P Bross, S Udvari, et al.
Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.
Translational Psychiatry|February 15, 2017
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorderF Lescai, T D Als, Q Li, et al.
American Journal of Human Genetics|February 11, 1999
Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, B J Poorthuis, et al.
Experimental Gerontology|August 30, 2011
Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) projectA Skytthe, S Valensin, B Jeune, et al.
Diabetologia|November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesA Albrechtsen, N Grarup, Y Li, et al.
Pageof 15

Showing results (141-150 of 146) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 146 results.
Human Molecular Genetics|May 1, 1997
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?B S Andresen, P Bross, S Udvari, et al.
Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.
Translational Psychiatry|February 15, 2017
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorderF Lescai, T D Als, Q Li, et al.
American Journal of Human Genetics|February 11, 1999
Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, B J Poorthuis, et al.
Experimental Gerontology|August 30, 2011
Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) projectA Skytthe, S Valensin, B Jeune, et al.
Diabetologia|November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesA Albrechtsen, N Grarup, Y Li, et al.
Pageof 15