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Biology / Galactosemia / Galactose-1-phosphate uridylyltransferase deficiency / Galactose—1-phosphate uridylyltransferase / Galactokinase deficiency / Galactokinase / Galactose / UDP-glucose 4-epimerase / Galactosemic cataract / Inborn errors of carbohydrate metabolism / Health / Medicine


May[removed]Volume 30 Number 5 Feature
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Document Date: 2010-04-29 15:46:04


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City

Los Angeles / Duarte / /

Company

Mayo Medical Laboratories / IgG / Conclusion Laboratory / The Biochemical Genetics Laboratory / /

Country

United States / /

Currency

pence / /

Facility

Appropriate laboratory / /

IndustryTerm

energy production / carrier detection / dairy products / chemical / carrier status / treatment for galactosemia / energy / /

MedicalCondition

classic galactosemia / autosomal recessive genetic disorder / Leukemia / minimal residual disease / cancer / cataracts / disease / premature ovarian failure / Chronic Lymphocytic Leukemia / Test Selection Galactosemia / galactosemia diagnosis / Amyloidosis / Feature Galactosemia / Galactosemia / vomiting / deafness / osteoporosis / Molecular Genetics Classic galactosemia / diarrhea / galactosemia alleles / Chronic myeloid leukemia / deficiency / galactosemia exhibit / galactosemia targets dietary restriction / MS / liver disease / meningitis / sepsis / suspected galactosemia / disorders / /

MedicalTreatment

blood transfusion / counseling / drug therapy / /

Person

Gordon W. Dewald / Hagop M. Kantarjian / Michael J. Mauro / Mark L. Litzow / Jorge Cortes / Moshe Talpaz / /

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Position

Major / genetic counselor / laboratory director / /

Product

thrive / Testosterone / Beta-2 / /

ProgrammingLanguage

R / /

ProvinceOrState

Louisiana / /

Technology

electrophoresis / Galactosemia Confirmation Algorithm / Antibodies / Hybridization / ATM / Genotyping / genotype / UDP / Gene Analysis / /

URL

www.mayoreferenceservices.org/communique / http /

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