Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 196 for BA 1
  1. PARK7 gene 
    ... Jun 26. Citation on PubMed Bonifati V, Oostra BA, Heutink P. Linking DJ-1 to neurodegeneration offers novel insights for understanding the ... Brice A, Meco G, van Duijn CM, Oostra BA, Heutink P. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. ...
    https://medlineplus.gov/genetics/gene/park7 - Genetics
  2. Neurofibromatosis type 1 
    ... spen.2006.01.005. Citation on PubMed Ward BA, Gutmann DH. Neurofibromatosis 1: from lab bench to clinic. Pediatr Neurol. 2005 ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  3. NF1 gene 
    ... PubMed or Free article on PubMed Central Ward BA, Gutmann DH. Neurofibromatosis 1: from lab bench to clinic. Pediatr Neurol. 2005 ...
    https://medlineplus.gov/genetics/gene/nf1 - Genetics
  4. Lafora progressive myoclonus epilepsy 
    ... 1; MELF1 PubMed Andrade DM, Turnbull J, Minassian BA. Lafora disease, seizures and sugars. Acta Myol. 2007 Jul;26(1):83-6. Citation on PubMed or Free article ...
    https://medlineplus.gov/.../lafora-progressive-myoclonus-epilepsy - Genetics
  5. Glucose-galactose malabsorption 
    ... j.ajg.2014.01.004. Epub 2014 Feb 1. Citation on PubMed Wright EM, Hirayama BA, Loo DF. Active sugar transport in health and disease. J Intern Med. 2007 Jan;261(1):32-43. doi: 10.1111/j.1365-2796. ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  6. GAA gene 
    ... Hoefsloot LH, Hoogeveen-Westerveld M, Reuser AJ, Oostra BA. Characterization of the human lysosomal alpha-glucosidase gene. Biochem J. 1990 Dec 1;272(2):493-7. doi: 10.1042/bj2720493. ...
    https://medlineplus.gov/genetics/gene/gaa - Genetics
  7. FOXL2 gene 
    ... Georges A, L'Hote D, Todeschini AL, Benayoun BA, Veitia RA. The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology. Mol Cell Endocrinol. 2012 Jun 5;356(1-2):55-64. doi: 10.1016/j.mce. ...
    https://medlineplus.gov/genetics/gene/foxl2 - Genetics
  8. PCBD1 gene 
    ... of PCBD1 PubMed PTERIN-4-ALPHA-CARBINOLAMINE DEHYDRATASE 1; PCBD1 NCBI Gene ClinVar Citron BA, Kaufman S, Milstien S, Naylor EW, Greene CL, ...
    https://medlineplus.gov/genetics/gene/pcbd1 - Genetics
  9. Laing distal myopathy 
    ... National Organization for Rare Disorders (NORD) MYOPATHY, DISTAL, 1; MPD1 PubMed Laing NG, Laing BA, Meredith C, Wilton SD, Robbins P, Honeyman K, ...
    https://medlineplus.gov/genetics/condition/laing-distal-myopathy - Genetics
  10. Congenital central hypoventilation syndrome 
    ... Disorders (NORD) ClinicalTrials.gov CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 1; CCHS1 PubMed Antic NA, Malow BA, Lange N, McEvoy RD, Olson AL, Turkington P, ...
    https://medlineplus.gov/...ngenital-central-hypoventilation-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next