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Results 1 - 10 of 35 for SN 2
  1. Hypertension 
    ... HYT8 HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 7 PubMed Dodoo SN, Benjamin IJ. Genomic Approaches to Hypertension. Cardiol Clin. 2017 May;35(2):185-196. doi: 10.1016/j.ccl.2016. ...
    https://medlineplus.gov/genetics/condition/hypertension - Genetics
  2. Familial glucocorticoid deficiency 
    ... Central Chung TT, Webb TR, Chan LF, Cooray SN, Metherell LA, King PJ, Chapple JP, Clark AJ. The majority of adrenocorticotropin receptor (melanocortin 2 receptor) mutations found in familial glucocorticoid deficiency type ...
    https://medlineplus.gov/.../familial-glucocorticoid-deficiency - Genetics
  3. Diamond-Blackfan anemia 
    ... science.aan2755. Citation on PubMed Narla A, Hurst SN, Ebert BL. Ribosome defects in disorders of erythropoiesis. Int J Hematol. 2011 Feb;93(2):144-149. doi: 10.1007/s12185-011-0776- ...
    https://medlineplus.gov/genetics/condition/diamond-blackfan-anemia - Genetics
  4. 22q11.2 deletion syndrome 
    ... Citation on PubMed Vorstman JAS, Morcus MEJ, Duijff SN, Klaassen PWJ, Heineman-de Boer JA, Beemer FA, Swaab H, Kahn RS, van Engeland H. The 22q11.2 deletion in children: high rate of autistic disorders ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  5. Jacobsen syndrome 
    ... gov JACOBSEN SYNDROME; JBS PubMed Akshoomoff N, Mattson SN, Grossfeld PD. Evidence for autism spectrum disorder in Jacobsen syndrome: identification of a candidate gene in distal 11q. Genet Med. 2015 Feb;17(2):143-8. doi: 10.1038/gim.2014.86. ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  6. Familial exudative vitreoretinopathy 
    ... Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, Moon RT, Hayden MR, Goldberg YP, Samuels ME. Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. Nat Genet. 2002 Oct;32(2):326-30. doi: 10.1038/ng957. Epub 2002 ...
    https://medlineplus.gov/.../familial-exudative-vitreoretinopathy - Genetics
  7. Polymicrogyria 
    ... N, Kimonis V, Lin JP, Lynch DR, Mohammed SN, Massey RF, McDonald M, Rogers RC, Splitt M, Stevens CA, Tischkowitz MD, Stoodley N, Leventer RJ, Pilz DT, Dobyns WB. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  8. 3-M syndrome 
    ... THREE M SYNDROME 3; 3M3 THREE M SYNDROME 2; 3M2 PubMed Clayton PE, Hanson D, Magee L, Murray PG, Saunders E, Abu-Amero SN, Moore GE, Black GC. Exploring the spectrum of ...
    https://medlineplus.gov/genetics/condition/3-m-syndrome - Genetics
  9. Kawasaki disease 
    ... NK, Wu CS, Yeh SZ, Chen CA, Chiu SN, Wu MH. Clinical Implication of the C Allele of the ITPKC Gene SNP rs28493229 in Kawasaki Disease: Association With Disease Susceptibility and BCG Scar Reactivation. Pediatr Infect Dis J. 2011 Feb;30(2):148-52. doi: 10.1097/INF.0b013e3181f43a4e. Citation ...
    https://medlineplus.gov/genetics/condition/kawasaki-disease - Genetics
  10. Perrault syndrome 
    ... 5; PRLTS5 PERRAULT SYNDROME 3; PRLTS3 PERRAULT SYNDROME 2; PRLTS2 PubMed Jenkinson EM, Rehman AU, Walsh T, Clayton-Smith J, Lee K, Morell RJ, Drummond MC, Khan SN, Naeem MA, Rauf B, Billington N, Schultz JM, ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics
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