These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Williams-Beuren Syndrome: more or less? Segmental duplications and deletions in the Williams-Beuren syndrome region provide new insights into language development. Tassabehji M; Donnai D Eur J Hum Genet; 2006 May; 14(5):507-8. PubMed ID: 16523213 [No Abstract] [Full Text] [Related]
4. [William's syndrome]. Rubia Vila FJ An R Acad Nac Med (Madr); 2007; 124(2):349-59; discussion 359-60. PubMed ID: 18069600 [TBL] [Abstract][Full Text] [Related]
5. Behavioral phenotypes in genetic syndromes: genetic clues to human behavior. Cassidy SB; Morris CA Adv Pediatr; 2002; 49():59-86. PubMed ID: 12214780 [TBL] [Abstract][Full Text] [Related]
6. [Physician or seer? Very early diagnosis and prognosis. The example of William's syndrome]. Ollivier AM Arch Pediatr; 2000 Nov; 7(11):1221-7. PubMed ID: 11109951 [TBL] [Abstract][Full Text] [Related]
7. What can developmental disorders tell us about the neurocomputational constraints that shape development? The case of Williams syndrome. Karmiloff-Smith A; Thomas M Dev Psychopathol; 2003; 15(4):969-90. PubMed ID: 14984134 [TBL] [Abstract][Full Text] [Related]
8. Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder. Osborne LR Mol Genet Metab; 1999 May; 67(1):1-10. PubMed ID: 10329018 [No Abstract] [Full Text] [Related]
9. Severe eating disorder in a 28-year-old man with William's syndrome. Young T; Apfeldorf W; Knepper J; Yager J Am J Psychiatry; 2009 Jan; 166(1):25-31. PubMed ID: 19122015 [No Abstract] [Full Text] [Related]
10. [William's syndrome. Report of a case with family involvement]. Onís Vilches MC; Rubio Cuadrado MV; Martínez de la Iglesia J; López Granados A Rev Clin Esp; 1998 Feb; 198(2):91-4. PubMed ID: 9558923 [TBL] [Abstract][Full Text] [Related]
11. Outcome in adult life for people with Williams syndrome-- results from a survey of 239 families. Howlin P; Udwin O J Intellect Disabil Res; 2006 Feb; 50(Pt 2):151-60. PubMed ID: 16403203 [TBL] [Abstract][Full Text] [Related]
12. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations. Tassabehji M Hum Mol Genet; 2003 Oct; 12 Spec No 2():R229-37. PubMed ID: 12952863 [TBL] [Abstract][Full Text] [Related]
13. Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome. Wang MS; Schinzel A; Kotzot D; Balmer D; Casey R; Chodirker BN; Gyftodimou J; Petersen MB; Lopez-Rangel E; Robinson WP Am J Med Genet; 1999 Sep; 86(1):34-43. PubMed ID: 10440826 [TBL] [Abstract][Full Text] [Related]
14. Autism and Williams syndrome: a case report. Herguner S; Mukaddes NM World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145 [TBL] [Abstract][Full Text] [Related]
15. Verbal and nonverbal abilities in the Williams syndrome phenotype: evidence for diverging developmental trajectories. Jarrold C; Baddeley AD; Hewes AK J Child Psychol Psychiatry; 1998 May; 39(4):511-23. PubMed ID: 9599779 [TBL] [Abstract][Full Text] [Related]
16. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes. Botta A; Novelli G; Mari A; Novelli A; Sabani M; Korenberg J; Osborne LR; Digilio MC; Giannotti A; Dallapiccola B J Med Genet; 1999 Jun; 36(6):478-80. PubMed ID: 10874638 [TBL] [Abstract][Full Text] [Related]
17. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome]. Milà M; Carrió A; Sánchez A; Gómez D; Jiménez D; Estivill X; Ballesta F Med Clin (Barc); 1999 Jun; 113(2):46-9. PubMed ID: 10425618 [TBL] [Abstract][Full Text] [Related]
18. [Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects]. van Hagen JM; Govaerts LC; de Coo IF; Gille JJ; Nieuwint AW; Madan K Ned Tijdschr Geneeskd; 2001 Mar; 145(9):396-400. PubMed ID: 11253493 [TBL] [Abstract][Full Text] [Related]
19. [Magnetic resonance features of supravalvular aortic stenosis in William's syndrome. Report of 2 cases]. Di Cesare E; Sabatini M; Splendiani A; Masciocchi C Radiol Med; 1998; 96(1-2):113-5. PubMed ID: 9819633 [No Abstract] [Full Text] [Related]
20. Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype. Martens MA; Wilson SJ; Reutens DC J Child Psychol Psychiatry; 2008 Jun; 49(6):576-608. PubMed ID: 18489677 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]