Morris CA - Search Results

1

The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptoms.

Tam E, Young EJ, Morris CA, Marshall CR, Loo W, Scherer SW, Mervis CB, Osborne LR. Tam E, et al. Among authors: morris ca. Am J Med Genet A. 2008 Jul 15;146A(14):1797-806. doi: 10.1002/ajmg.a.32360. Am J Med Genet A. 2008. PMID: 18553513 Free PMC article.

2

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition.

Frangiskakis JM, Ewart AK, Morris CA, Mervis CB, Bertrand J, Robinson BF, Klein BP, Ensing GJ, Everett LA, Green ED, Pröschel C, Gutowski NJ, Noble M, Atkinson DL, Odelberg SJ, Keating MT. Frangiskakis JM, et al. Among authors: morris ca. Cell. 1996 Jul 12;86(1):59-69. doi: 10.1016/s0092-8674(00)80077-x. Cell. 1996. PMID: 8689688 Free article.

3

The Williams syndrome cognitive profile.

Mervis CB, Robinson BF, Bertrand J, Morris CA, Klein-Tasman BP, Armstrong SC. Mervis CB, et al. Among authors: morris ca. Brain Cogn. 2000 Dec;44(3):604-28. doi: 10.1006/brcg.2000.1232. Brain Cogn. 2000. PMID: 11104544

4

Williams syndrome and related disorders.

Morris CA, Mervis CB. Morris CA, et al. Annu Rev Genomics Hum Genet. 2000;1:461-84. doi: 10.1146/annurev.genom.1.1.461. Annu Rev Genomics Hum Genet. 2000. PMID: 11701637 Review.

5

Attentional characteristics of infants and toddlers with Williams syndrome during triadic interactions.

Mervis CB, Morris CA, Klein-Tasman BP, Bertrand J, Kwitny S, Appelbaum LG, Rice CE. Mervis CB, et al. Among authors: morris ca. Dev Neuropsychol. 2003;23(1-2):243-68. doi: 10.1080/87565641.2003.9651894. Dev Neuropsychol. 2003. PMID: 12730027

6

Heat shock protein 27 gene: chromosomal and molecular location and relationship to Williams syndrome.

Stock AD, Spallone PA, Dennis TR, Netski D, Morris CA, Mervis CB, Hobart HH. Stock AD, et al. Among authors: morris ca. Am J Med Genet A. 2003 Jul 30;120A(3):320-5. doi: 10.1002/ajmg.a.20055. Am J Med Genet A. 2003. PMID: 12838549

7

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.

Morris CA, Mervis CB, Hobart HH, Gregg RG, Bertrand J, Ensing GJ, Sommer A, Moore CA, Hopkin RJ, Spallone PA, Keating MT, Osborne L, Kimberley KW, Stock AD. Morris CA, et al. Am J Med Genet A. 2003 Nov 15;123A(1):45-59. doi: 10.1002/ajmg.a.20496. Am J Med Genet A. 2003. PMID: 14556246

8

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome.

Meyer-Lindenberg A, Kohn P, Mervis CB, Kippenhan JS, Olsen RK, Morris CA, Berman KF. Meyer-Lindenberg A, et al. Among authors: morris ca. Neuron. 2004 Sep 2;43(5):623-31. doi: 10.1016/j.neuron.2004.08.014. Neuron. 2004. PMID: 15339645 Free article.

9

Intellectual abilities and adaptive behavior of children and adolescents with Kabuki syndrome: a preliminary study.

Mervis CB, Becerra AM, Rowe ML, Hersh JH, Morris CA. Mervis CB, et al. Among authors: morris ca. Am J Med Genet A. 2005 Jan 30;132A(3):248-55. doi: 10.1002/ajmg.a.30334. Am J Med Genet A. 2005. PMID: 15523605

10

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

Meyer-Lindenberg A, Mervis CB, Sarpal D, Koch P, Steele S, Kohn P, Marenco S, Morris CA, Das S, Kippenhan S, Mattay VS, Weinberger DR, Berman KF. Meyer-Lindenberg A, et al. Among authors: morris ca. J Clin Invest. 2005 Jul;115(7):1888-95. doi: 10.1172/JCI24892. Epub 2005 Jun 9. J Clin Invest. 2005. PMID: 15951840 Free PMC article.

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