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Showing results (81-90 of 85) with videos related to

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American Journal of Medical Genetics|July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18qJ D Cody, P D Ghidoni, B R DuPont, et al.
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.
Pediatric Obesity|November 19, 2014
Metabolites as novel biomarkers for childhood obesity-related traits in Mexican-American childrenV S Farook, L Reddivari, G Chittoor, et al.
Human Molecular Genetics|May 16, 1998
Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduriaN Gregersen, V S Winter, M J Corydon, et al.
Molecular Human Reproduction|May 22, 2013
Localization of a major susceptibility locus influencing preterm birthG Chittoor, V S Farook, S Puppala, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
American Journal of Medical Genetics|July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18qJ D Cody, P D Ghidoni, B R DuPont, et al.
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.
Pediatric Obesity|November 19, 2014
Metabolites as novel biomarkers for childhood obesity-related traits in Mexican-American childrenV S Farook, L Reddivari, G Chittoor, et al.
Human Molecular Genetics|May 16, 1998
Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduriaN Gregersen, V S Winter, M J Corydon, et al.
Molecular Human Reproduction|May 22, 2013
Localization of a major susceptibility locus influencing preterm birthG Chittoor, V S Farook, S Puppala, et al.
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