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Results 1 - 10 of 12 for Williams syndrome
  1. ... because its deletion causes a different disorder called Williams syndrome (described below), also known as Williams-Beuren syndrome. ... these additional features. More About This Health Condition Williams syndrome is caused by the deletion of genetic material ...
  2. ... 565. Citation on PubMed Cassidy SB, Dykens E, Williams CA. Prader-Willi and Angelman syndromes: sister imprinted disorders. Am J Med Genet. 2000 ...
  3. ... Xu S, Han JC, Morales A, Menzie CM, Williams K, Fan YS. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to ...
  4. ... article on PubMed Central UCSC Genome Browser: Statistics ... syndrome, with brachydactyly type E, developmental delays, and behavioral ...
  5. ... Whitehead SL, Whittaker P, Willey DL, Williams L, Williams SA, Wilming L, Wray ... patients with myelodysplastic syndrome (MDS): a study of the Greek MDS Study ...
  6. ... a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N Engl ... Hayne CC, Winer E, Williams T, Chaves F, Khorsand J, Mark HF. Acute ...
  7. ... Whiteley MN, Wilkinson JE, Willey DL, Williams G, Williams L, Williamson A, ... syndromes: not just variants of Klinefelter syndrome. Acta Paediatr. ...
  8. ... Wallis JM, West AP, Whitehead SL, Willey DL, Williams SA, Wilming L, Wray PW, ... metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. ...
  9. ... White S, Whitehead SL, Wilkinson JE, Willey DL, Williams H, Wilming L, Wray PW, ... clinical characterization of the syndrome. Am J Hum Genet. 2003 May;72(5): ...
  10. ... Ulanovsky LE, Ustaszewska A, Vo N, White PS, Williams AL, Wills PL, Wu JR, Wu ... Rubinstein-Taybi syndrome: an update of the CREBBP deletion repertoire. Hum ...
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