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Louis J Elsas

Showing results (11-20 of 15) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2004
Cystathionine beta-synthase deficiency: effects of betaine supplementation after methionine restriction in B6-nonresponsive homocystinuriaRani H Singh, Warren D Kruger, Liqun Wang, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Gaucher disease: in vivo evidence for allele dose leading to neuronopathic and nonneuronopathic phenotypesHuiquan Zhao, Laurie A Bailey, Louis J Elsas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2004
Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptorsPhyllis B Acosta, Steven Yannicelli, Rani H Singh, et al.
Pediatric Research|October 25, 2007
Screening newborns for galactosemia using total body galactose oxidation to CO2 in expired airDeborah S Barbouth, Darcy L Velazquez, Stanley Konopka, et al.
Human Mutation|July 11, 2007
Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridizationYao-Shan Fan, Parul Jayakar, Hongbo Zhu, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2004
Cystathionine beta-synthase deficiency: effects of betaine supplementation after methionine restriction in B6-nonresponsive homocystinuriaRani H Singh, Warren D Kruger, Liqun Wang, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Gaucher disease: in vivo evidence for allele dose leading to neuronopathic and nonneuronopathic phenotypesHuiquan Zhao, Laurie A Bailey, Louis J Elsas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2004
Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptorsPhyllis B Acosta, Steven Yannicelli, Rani H Singh, et al.
Pediatric Research|October 25, 2007
Screening newborns for galactosemia using total body galactose oxidation to CO2 in expired airDeborah S Barbouth, Darcy L Velazquez, Stanley Konopka, et al.
Human Mutation|July 11, 2007
Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridizationYao-Shan Fan, Parul Jayakar, Hongbo Zhu, et al.
Pageof 2