4.5 Article

Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Pediatrics

Diverticulitis in a child with Williams syndrome: a case report and review of the literature

Romeo C. Ignacio et al.

JOURNAL OF PEDIATRIC SURGERY (2012)

Article Education, Special

MRI amygdala volume in Williams Syndrome

Liliana Capitao et al.

RESEARCH IN DEVELOPMENTAL DISABILITIES (2011)

Article Genetics & Heredity

Essential role of the N-terminal region of TFII-I in viability and behavior

Jaume Lucena et al.

BMC MEDICAL GENETICS (2010)

Review Medicine, General & Internal

MEDICAL PROGRESS Williams-Beuren Syndrome

Barbara R. Pober

NEW ENGLAND JOURNAL OF MEDICINE (2010)

Review Biochemistry & Molecular Biology

The genomic basis of the Williams - Beuren syndrome

C. Schubert

CELLULAR AND MOLECULAR LIFE SCIENCES (2009)

Article Medicine, Research & Experimental

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

Hong Hua Li et al.

EMBO MOLECULAR MEDICINE (2009)

Review Clinical Neurology

Brain abnormalities in Williams syndrome: A review of structural and functional magnetic resonance imaging findings

Andrea Parolin Jackowski et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (2009)

Article Multidisciplinary Sciences

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

Badam Enkhmandakh et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Article Multidisciplinary Sciences

被撤回的出版物: Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF) (Retracted article. See vol. 111, pg. 2398, 2014)

Kimihiro Yoshimura et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Review Psychology, Developmental

Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype

Marilee A. Martens et al.

JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2008)

Review Medicine, Research & Experimental

Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome

Barbara R. Pober et al.

JOURNAL OF CLINICAL INVESTIGATION (2008)

Review Behavioral Sciences

Fronto-parietal and cerebellar contributions to motor dysfunction in Williams syndrome: A review and future directions

Darren R. Hocking et al.

NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2008)

Review Psychology, Developmental

Defining the social phenotype in Williams syndrome:: A model for linking gene, the brain, and behavior

Anna Jarvinen-Pasley et al.

DEVELOPMENT AND PSYCHOPATHOLOGY (2008)

Article Clinical Neurology

Evolution of neurologic features in Williams syndrome

Chiara Gagliardi et al.

PEDIATRIC NEUROLOGY (2007)

Review Clinical Neurology

Language and communicative development in Williams syndrome

Carolyn B. Mervis et al.

MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2007)

Article Genetics & Heredity

Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension

M Del Campo et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2006)

Article Genetics & Heredity

Discriminating power of localized three-dimensional facial morphology

P Hammond et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2005)

Article Multidisciplinary Sciences

GTF2IRD1 in craniofacial development of humans and mice

M Tassabehji et al.

SCIENCE (2005)

Article Genetics & Heredity

Sensorineural hearing loss in children and adults with Williams syndrome

JA Marler et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)

Article Medicine, Research & Experimental

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

A Meyer-Lindenberg et al.

JOURNAL OF CLINICAL INVESTIGATION (2005)

Article Dentistry, Oral Surgery & Medicine

Neurocranial morphology and growth in Williams syndrome

S Axelsson et al.

EUROPEAN JOURNAL OF ORTHODONTICS (2005)

Article Genetics & Heredity

Everybody in the world is my friend hypersociability in young children with Williams syndrome

TF Doyle et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)

Article Genetics & Heredity

Mutational mechanisms of Williams-Beuren syndrome deletions

M Bayés et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)

Article Clinical Neurology

Williams syndrome - Neuronal size and neuronal-packing density in primary visual cortex

AM Galaburda et al.

ARCHIVES OF NEUROLOGY (2002)

Article Behavioral Sciences

Cholinergic activation of the basolateral amygdala regulates unlearned freezing behavior in rats

AE Power et al.

BEHAVIOURAL BRAIN RESEARCH (2002)

Article Clinical Neurology

Prevalence estimation of Williams syndrome

P Stromme et al.

JOURNAL OF CHILD NEUROLOGY (2002)

Article Neurosciences

The Williams syndrome cognitive profile

CB Mervis et al.

BRAIN AND COGNITION (2000)

Article Biochemistry & Molecular Biology

Elastin: mutational spectrum in supravalvular aortic stenosis

K Metcalfe et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2000)

Article Neurosciences

Neuroanatomy of Williams syndrome: A high-resolution MRI study

AL Reiss et al.

JOURNAL OF COGNITIVE NEUROSCIENCE (2000)

Article Genetics & Heredity

A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome-deletion region at 7q11.23

R Peoples et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)