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Results 1 - 10 of 12 for Perry syndrome
  1. Perry syndrome is a progressive brain disease that is characterized by four major features: a pattern of movement ...
  2. ... Delaney JW, Yetman AT, Hammel JM, Sanmann JN, Perry DA, Schaefer GB, Olney AH. Myhre syndrome: Clinical features and restrictive cardiopulmonary complications. Am J ...
  3. ... Li J, Lancaster J, Fox PT, Stratton RF, Perry B, Hale DE. Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay. Am J Med Genet ...
  4. ... J, Marinier E, Martinez-Vinson C, Peretti N, Perry A, Roquelaure B, Venaille A, Sarles J, Goulet O, Badens C. Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child. 2014 Jan;99(1):35- ...
  5. ... Jiang H, Evans S, Macgillivray C, Nightingale M, Perry S, Ferguson M, LeBlanc ... gene ORC4 cause Meier-Gorlin syndrome. Nat Genet. 2011 Feb 27;43(4):360- ...
  6. ... Organization for Rare Disorders (NORD) CHROMOSOME 18q DELETION SYNDROME PubMed Cody JD, Sebold C, Heard P, Carter E, Soileau B, Hasi-Zogaj M, Hill A, Rupert D, Perry B, O'Donnell L, Gelfond J, Lancaster J, ...
  7. ... encephalopathy-lactic acidosis-stroke Genetic Testing Registry: MELAS syndrome ... PubMed Betts J, Jaros E, Perry RH, Schaefer AM, Taylor RW, Abdel-All Z, ...
  8. ... Fisher M, Morrison H, Bicknell L, Gautier P, Perry P, Sokhi K, Sexton D, Bardakjian ... Anophthalmia) syndrome in humans and mice. PLoS Genet. 2011 Jul; ...
  9. ... Attenuated familial adenomatous polyposis Familial adenomatous polyposis Gardner syndrome ... Attard TM, Cuffari C, Tajouri T, Stoner JA, Eisenberg MT, Yardley JH, Abraham SC, Perry D, Vanderhoof J, Lynch H. Multicenter experience with ...
  10. ... Klein GJ, Law IH, Morady FJ, Paul T, Perry JC, Sanatani S, Tanel RE. PACES/HRS expert ...
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