Results 21 -
30
of
35
for
Marshall syndrome
- ... 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. ...
- ... Expanding the clinical phenotype of the 3q29 microdeletion syndrome and ... D, Sharkey FH, Lionel AC, Marshall CR, Azam T, Shago M, Chong K, Mendoza- ...
- ... autosomal recessive skin fragility and photosensitivity disorder, Kindler ... TM, Marinkovich MP, Marshall JF, McGrath JA, Mellerio JE, Polson R, Heagerty ...
- ... 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 ...
- ... 31256. Citation on PubMed Huang T, Lock JE, Marshall AC, ... clinical criteria for Holt-Oram syndrome. Pediatr Res. 2005 Nov;58(5):981-6. ...
- ... PubMed Central Visootsak J, Graham JM Jr. Klinefelter syndrome ... Waters PD, Wallis MC, Marshall Graves JA. Mammalian sex--Origin and evolution of ...
- ... Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS. ... syndrome associated with mental retardation and seizures. Nat Genet. ...
- ... of XK PubMed ... WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker ...
- ... 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 ...
- ... Disorders (NORD) ClinicalTrials.gov ... Dolcetti A, Silversides CK, Marshall CR, Lionel AC, Stavropoulos DJ, Scherer SW, Bassett ...