262 related articles for article (PubMed ID: 30375319)
21. Fading-figure tracing in Williams syndrome.
Nagai C; Inui T; Iwata M
Brain Cogn; 2011 Feb; 75(1):10-7. PubMed ID: 21074925
[TBL] [Abstract][Full Text] [Related]
22. Chromosomal Microarray Analysis in Taiwanese Patients with Williams-Beuren Syndrome.
Kuo HT; Chen CH; Lin CY; Chang YS; Chang JG
Cytogenet Genome Res; 2019; 159(4):182-189. PubMed ID: 31931504
[TBL] [Abstract][Full Text] [Related]
23. Mosaic Williams syndrome: A case report.
Kalantari S; Biagio MD; Valente EM; Rossi E; Sirchia F
Am J Med Genet A; 2023 Jan; 191(1):249-252. PubMed ID: 36263864
[TBL] [Abstract][Full Text] [Related]
24. Cognitive and behavioral characteristics of children with Williams syndrome: implications for intervention approaches.
Mervis CB; John AE
Am J Med Genet C Semin Med Genet; 2010 May; 154C(2):229-48. PubMed ID: 20425784
[TBL] [Abstract][Full Text] [Related]
25. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays.
Dai L; Bellugi U; Chen XN; Pulst-Korenberg AM; Järvinen-Pasley A; Tirosh-Wagner T; Eis PS; Graham J; Mills D; Searcy Y; Korenberg JR
Am J Med Genet A; 2009 Mar; 149A(3):302-14. PubMed ID: 19205026
[TBL] [Abstract][Full Text] [Related]
26. Williams syndrome: a genetic deletion disorder presenting clues to the biology of sociability and clinical challenges of hypersociability.
Deutsch SI; Rosse RB; Schwartz BL
CNS Spectr; 2007 Dec; 12(12):903-7. PubMed ID: 18163035
[TBL] [Abstract][Full Text] [Related]
27. Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population.
Crespi BJ; Hurd PL
BMC Neurosci; 2014 Nov; 15():127. PubMed ID: 25429715
[TBL] [Abstract][Full Text] [Related]
28. Cognitive, lexical and morpho-syntactic profiles of Israeli children with Williams syndrome.
Levy Y; Bechar T
Cortex; 2003 Apr; 39(2):255-71. PubMed ID: 12784888
[TBL] [Abstract][Full Text] [Related]
29. "Everybody in the world is my friend" hypersociability in young children with Williams syndrome.
Doyle TF; Bellugi U; Korenberg JR; Graham J
Am J Med Genet A; 2004 Jan; 124A(3):263-73. PubMed ID: 14708099
[TBL] [Abstract][Full Text] [Related]
30. Neuropsychological profile of Italians with Williams syndrome: an example of a dissociation between language and cognition?
Vicari S; Bates E; Caselli MC; Pasqualetti P; Gagliardi C; Tonucci F; Volterra V
J Int Neuropsychol Soc; 2004 Oct; 10(6):862-76. PubMed ID: 15637777
[TBL] [Abstract][Full Text] [Related]
31. Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome.
Hoeft F; Dai L; Haas BW; Sheau K; Mimura M; Mills D; Galaburda A; Bellugi U; Korenberg JR; Reiss AL
PLoS One; 2014; 9(8):e104088. PubMed ID: 25105779
[TBL] [Abstract][Full Text] [Related]
32. Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.
Kopp ND; Parrish PCR; Lugo M; Dougherty JD; Kozel BA
Mol Genet Genomic Med; 2018 Sep; 6(5):749-765. PubMed ID: 30008175
[TBL] [Abstract][Full Text] [Related]
33. GTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeats.
Makeyev AV; Erdenechimeg L; Mungunsukh O; Roth JJ; Enkhmandakh B; Ruddle FH; Bayarsaihan D
Proc Natl Acad Sci U S A; 2004 Jul; 101(30):11052-7. PubMed ID: 15243160
[TBL] [Abstract][Full Text] [Related]
34. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.
Meng X; Lu X; Li Z; Green ED; Massa H; Trask BJ; Morris CA; Keating MT
Hum Genet; 1998 Nov; 103(5):590-9. PubMed ID: 9860302
[TBL] [Abstract][Full Text] [Related]
35. Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.
Hinsley TA; Cunliffe P; Tipney HJ; Brass A; Tassabehji M
Protein Sci; 2004 Oct; 13(10):2588-99. PubMed ID: 15388857
[TBL] [Abstract][Full Text] [Related]
36. The neurobiology of Williams syndrome: cascading influences of visual system impairment?
Eckert MA; Galaburda AM; Mills DL; Bellugi U; Korenberg JR; Reiss AL
Cell Mol Life Sci; 2006 Aug; 63(16):1867-75. PubMed ID: 16810457
[TBL] [Abstract][Full Text] [Related]
37. Neurodevelopmental and behavioral issues in Williams syndrome.
Paterson SJ; Schultz RT
Curr Psychiatry Rep; 2007 Apr; 9(2):165-71. PubMed ID: 17389129
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. The Association of Intelligence, Visual-Motor Functioning, and Personality Characteristics With Adaptive Behavior in Individuals With Williams Syndrome.
Fu TJ; Lincoln AJ; Bellugi U; Searcy YM
Am J Intellect Dev Disabil; 2015 Jul; 120(4):273-88. PubMed ID: 26161466
[TBL] [Abstract][Full Text] [Related]
40. Williams syndrome: a relationship between genetics, brain morphology and behaviour.
Fahim C; Yoon U; Nashaat NH; Khalil AK; El-Belbesy M; Mancini-Marie A; Evans AC; Meguid N
J Intellect Disabil Res; 2012 Sep; 56(9):879-94. PubMed ID: 22044458
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]