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Results 1 - 10 of 213 for scs
  1. Roberts syndrome 
    ... individuals may live into adulthood. A condition called SC phocomelia syndrome was originally thought to be distinct ... is now considered to be a mild variant. "SC" represents the first letters of the surnames of ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  2. TWIST1 gene 
    ... B-HLH DNA binding protein CRS1 H-twist SCS Transcription factor TWIST TWIST twist basic helix-loop- ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  3. SUCLA2 gene 
    ... beta subunit renal carcinoma antigen NY-REN-39 SCS-betaA SUCB1_HUMAN succinate-CoA ligase beta subunit ...
    https://medlineplus.gov/genetics/gene/sucla2 - Genetics
  4. FGFR2 gene 
    ... FACTOR RECEPTOR 2; FGFR2 NCBI Gene ClinVar Azoury SC, Reddy S, Shukla V, Deng CX. Fibroblast Growth ... 16(3):361-8. doi: 10.1097/01.scs.0000157078.53871.11. Citation on PubMed Chokdeemboon C, ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  5. Hypokalemic periodic paralysis 
    ... HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2 PubMed Cannon SC. An expanding view for the molecular basis of ... 8966(02)00007-x. Citation on PubMed Cannon SC. Channelopathies of skeletal muscle excitability. Compr Physiol. 2015 ...
    https://medlineplus.gov/.../condition/hypokalemic-periodic-paralysis - Genetics
  6. Narcolepsy 
    ... G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Honda Y, Honda M, Hogl B, Longstreth WT ... X, Winkelmann J, Plazzi G, Nevsimalova S, Hong SC, Honda Y, Honda M, Hogl B, Ton TG, ...
    https://medlineplus.gov/genetics/condition/narcolepsy - Genetics
  7. 3-methylcrotonyl-CoA carboxylase deficiency 
    ... PubMed or Free article on PubMed Central Grunert SC, Stucki M, Morscher RJ, Suormala T, Burer C, ... Epub 2014 Nov 6. Citation on PubMed Stadler SC, Polanetz R, Maier EM, Heidenreich SC, Niederer B, ...
    https://medlineplus.gov/...methylcrotonyl-coa-carboxylase-deficiency - Genetics
  8. Stevens-Johnson syndrome/toxic epidermal necrolysis 
    ... Mar 5. Citation on PubMed Cheng CY, Su SC, Chen CH, Chen WL, Deng ST, Chung WH. ... Central Chung WH, Hung SI, Yang JY, Su SC, Huang SP, Wei CY, Chin SW, Chiou CC, ...
    https://medlineplus.gov/...hnson-syndrome-toxic-epidermal-necrolysis - Genetics
  9. Menkes syndrome 
    ... on PubMed Central Donsante A, Tang J, Godwin SC, Holmes CS, Goldstein DS, Bassuk A, Kaler SG. ... SG, Holmes CS, Goldstein DS, Tang J, Godwin SC, Donsante A, Liew CJ, Sato S, Patronas N. ...
    https://medlineplus.gov/genetics/condition/menkes-syndrome - Genetics
  10. MCCC1 gene 
    ... PubMed or Free article on PubMed Central Grunert SC, Stucki M, Morscher RJ, Suormala T, Burer C, ... 1006/geno.2000.6366. Citation on PubMed Stadler SC, Polanetz R, Maier EM, Heidenreich SC, Niederer B, ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
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