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Results 21 - 30 of 35 for Marshall syndrome
  1. ... 3. Citation on PubMed Dolcetti A, Silversides CK, Marshall CR, ... KL, Shaffer LG. Monosomy 1p36 deletion syndrome. Am J Med Genet C Semin Med Genet. ...
  2. ... Expanding the clinical phenotype of the 3q29 microdeletion syndrome and ... D, Sharkey FH, Lionel AC, Marshall CR, Azam T, Shago M, Chong K, Mendoza- ...
  3. ... autosomal recessive skin fragility and photosensitivity disorder, Kindler ... TM, Marinkovich MP, Marshall JF, McGrath JA, Mellerio JE, Polson R, Heagerty ...
  4. ... Knijnenburg J, Fitzpatrick D, Sharkey FH, Lionel AC, Marshall CR, Azam T, Shago ... microduplication: a new syndrome in a three-generation family. Am J Med ...
  5. ... 31256. Citation on PubMed Huang T, Lock JE, Marshall AC, ... clinical criteria for Holt-Oram syndrome. Pediatr Res. 2005 Nov;58(5):981-6. ...
  6. ... PubMed Central Visootsak J, Graham JM Jr. Klinefelter syndrome ... Waters PD, Wallis MC, Marshall Graves JA. Mammalian sex--Origin and evolution of ...
  7. ... Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS. ... syndrome associated with mental retardation and seizures. Nat Genet. ...
  8. ... of XK PubMed ... WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker ...
  9. ... Condition MedlinePlus Genetics provides information about Lennox-Gastaut syndrome More About ... A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold ...
  10. ... Disorders (NORD) ClinicalTrials.gov ... Dolcetti A, Silversides CK, Marshall CR, Lionel AC, Stavropoulos DJ, Scherer SW, Bassett ...
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