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Items: 1 to 20 of 21

1.

Introduction: Williams syndrome.

Morris CA.

Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):203-8. doi: 10.1002/ajmg.c.30266.

2.

Description of common musculoskeletal findings in Williams Syndrome and implications for therapies.

Copes LE, Pober BR, Terilli CA.

Clin Anat. 2016 Jul;29(5):578-89. doi: 10.1002/ca.22685. Epub 2016 Jan 25. Review.

PMID:
26749433
3.

Williams syndrome and related disorders.

Morris CA, Mervis CB.

Annu Rev Genomics Hum Genet. 2000;1:461-84. Review.

PMID:
11701637
4.

Stroke in Williams syndrome.

Wollack JB, Kaifer M, LaMonte MP, Rothman M.

Stroke. 1996 Jan;27(1):143-6. Review.

5.

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.

Meyer-Lindenberg A, Mervis CB, Berman KF.

Nat Rev Neurosci. 2006 May;7(5):380-93. Review.

PMID:
16760918
6.

[Investigating the "social brain" through Williams syndrome].

Nagamine M, Mimura M, Reiss AL, Hoeft F.

Brain Nerve. 2010 Aug;62(8):877-84. Review. Japanese.

PMID:
20714036
7.

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. doi: 10.1111/j.1469-7610.2008.01887.x. Review.

PMID:
18489677
8.

Language and communicative development in Williams syndrome.

Mervis CB, Becerra AM.

Ment Retard Dev Disabil Res Rev. 2007;13(1):3-15. Review.

PMID:
17326109
9.

[Williams syndrome: its clinical aspects and molecular bases].

Antonell A, Del Campo M, Flores R, Campuzano V, Perez-Jurado LA.

Rev Neurol. 2006 Jan 7;42 Suppl 1:S69-75. Review. Spanish.

10.

Elastin gene deletions in Williams syndrome.

Smoot LB.

Curr Opin Pediatr. 1995 Dec;7(6):698-701. Review.

PMID:
8776022
11.

[Williams syndrome].

Alleva E, Cirulli F, Calamandrei G, Rondinini C, Capirci O, Aloe L, Volterra V.

Ann Ist Super Sanita. 1999;35(2):211-9. Review. Italian.

PMID:
10645654
12.

Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.

Tassabehji M.

Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R229-37. Epub 2003 Sep 2. Review.

PMID:
12952863
13.

Familial Williams-Beuren syndrome showing varying clinical expression.

Pankau R, Siebert R, Kautza M, Schneppenheim R, Gosch A, Wessel A, Partsch CJ.

Am J Med Genet. 2001 Feb 1;98(4):324-9. Review.

PMID:
11170076
14.

[Genetic diagnosis of Williams syndrome].

Urbán Z, Kiss E, Kádár K, Szabolcs J, Csiszár K, Boyd DC, Fekete G.

Orv Hetil. 1997 Jul 6;138(27):1749-52. Review. Hungarian.

PMID:
9273487
15.

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.

Cassidy SB, Morris CA.

Adv Pediatr. 2002;49:59-86. Review.

PMID:
12214780
16.

Williams syndrome: from genotype through to the cognitive phenotype.

Donnai D, Karmiloff-Smith A.

Am J Med Genet. 2000 Summer;97(2):164-71. Review.

PMID:
11180224
17.

Brain imaging in neurogenetic conditions: realizing the potential of behavioral neurogenetics research.

Reiss AL, Eliez S, Schmitt JE, Patwardhan A, Haberecht M.

Ment Retard Dev Disabil Res Rev. 2000;6(3):186-97. Review.

PMID:
10982496
18.

The genomic basis of the Williams-Beuren syndrome.

Schubert C.

Cell Mol Life Sci. 2009 Apr;66(7):1178-97. doi: 10.1007/s00018-008-8401-y. Review.

PMID:
19039520
19.

Neurodevelopmental and behavioral issues in Williams syndrome.

Paterson SJ, Schultz RT.

Curr Psychiatry Rep. 2007 Apr;9(2):165-71. Review.

PMID:
17389129
20.

Williams syndrome: 15 years of psychological research.

Mervis CB.

Dev Neuropsychol. 2003;23(1-2):1-12. Review.

PMID:
12730017

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