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Results 1 - 10 of 34 for GAL 1
  1. Galactose-1-phosphate uridyltransferase is a blood test that measures the level of a substance called GALT, which helps break down milk sugars in your body. A low level of this substance causes a condition called galactosemia .
  2. ... its normal activity. More About This Health Condition Gal-1-P uridylyltransferase Galactosephosphate Uridylyltransferase GALT_HUMAN UDP Galactose ...
  3. Citizen's Guide to Pest Control and Pesticide Safety (Environmental Protection Agency) - PDF  
    Pesticides/Start Here ... Pesticides ... Environmental Protection Agency ... PDF ... pesticide,citizen's guide,pest control,pesticide safety
  4. ... 3; CSNBAD3 NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1 PubMed Gal A, Orth U, Baehr W, Schwinger E, Rosenberg ... 2010;664:263-72. doi: 10.1007/978-1-4419-1399-9_30. Citation on PubMed ... HJ, Rosenberg T, Gal A. p.Gln200Glu, a putative constitutively active mutant ...
  5. About Alpha-gal Syndrome (Centers for Disease Control and Prevention)  
    Food Allergy/Specifics ... Food Allergy ... Tick Bites/Specifics ... Tick Bites ... Centers for Disease Control and Prevention ... Alpha-gal syndrome can occur after certain types ...
  6. ... Bartsch O, von der Wense A, Meinecke P, Gal A. Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp. Cytogenet Genome Res. 2002;99(1-4):297-302. doi: 10.1159/000071607. Citation ...
  7. Food Allergy (American Academy of Allergy, Asthma, and Immunology)  
    Food Allergy/Start Here ... Food Allergy ... American Academy of Allergy, Asthma, and Immunology ... AAAAI, the experts in allergy and immunology, provide an overview ...
  8. ... Finckh U, Schroder J, Ressler B, Veske A, Gal A. Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am J Med Genet. 2000 May 1;92(1):40-6. doi: 10.1002/(sici) ...
  9. ... Finckh U, Schroder J, Ressler B, Veske A, Gal A. Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am J Med Genet. 2000 May 1;92(1):40-6. doi: 10.1002/(sici) ...
  10. ... C-Salcedo Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat Genet. 2001 Jan;27(1):108-12. doi: 10.1038/83667. Citation on ...
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