Published in Am J Med Genet on September 01, 1994
Rearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development. Expert Rev Mol Med (2007) 1.16
Second-order belief attribution in Williams syndrome: intact or impaired? Am J Ment Retard (1999) 0.91
Continuous cognitive dynamics of the evaluation of trustworthiness in williams syndrome. Front Psychol (2012) 0.90
Language and Literacy Development of Children with Williams Syndrome. Top Lang Disord (2009) 0.89
Verbal peaks and visual valleys in theory of mind ability in Williams syndrome. J Autism Dev Disord (2008) 0.77
Human versus non-human face processing: evidence from Williams syndrome. J Autism Dev Disord (2009) 0.76
Out with the Old and in with the New-Is Backward Inhibition a Domain-Specific Process? PLoS One (2015) 0.75
Calcium metabolism in Williams-Beuren syndrome. J Pediatr (1992) 1.41
Radioulnar synostosis in Williams-Beuren syndrome: a component manifestation. Am J Med Genet (1993) 1.39
Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome. Am J Med Genet (1994) 1.20
Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome. Dev Med Child Neurol (1997) 1.13
Social-emotional and behavioral adjustment in children with Williams-Beuren syndrome. Am J Med Genet (1994) 1.07
Anomalies of the abdominal aorta in Williams-Beuren syndrome--another cause of arterial hypertension. Eur J Pediatr (2001) 0.93
[Arterial hypertension and blood pressure profile in patients with Williams-Beuren syndrome]. Z Kardiol (1997) 0.91
Longitudinal evaluation of growth, puberty, and bone maturation in children with Williams syndrome. J Pediatr (1999) 0.90
Pediatric reference values of estradiol, testosterone, lutropin, follitropin and prolactin. Clin Lab (2000) 0.89
Normal growth and normalization of hypergonadotropic hypogonadism in atypical Turner syndrome (45,X/46,XX/47,XXX). Correlation of body height with distribution of cell lines. Eur J Pediatr (1994) 0.81
Longitudinal study of the cognitive development in children with Williams-Beuren syndrome. Am J Med Genet (1996) 0.81
The spectrum of ocular features in the Williams-Beuren syndrome. Clin Genet (1996) 0.80
Williams-Beuren syndrome and celiac disease. J Pediatr Gastroenterol Nutr (1996) 0.80
Sigmoid diverticulitis in patients with Williams-Beuren syndrome: relatively high prevalence and high complication rate in young adults with the syndrome. Am J Med Genet A (2005) 0.80
Adult patients with Prader-Willi syndrome: clinical characteristics, life circumstances and growth hormone secretion. Growth Horm IGF Res (2000) 0.79
"Autistic" behavior in two children with Williams-Beuren syndrome. Am J Med Genet (1994) 0.78
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism. Hum Genet (1993) 0.78
Diaphragmatic defect in Brachmann-de Lange syndrome: a further observation. Am J Med Genet (1993) 0.77
Hormonal regulation in children and adults with Williams-Beuren syndrome. Am J Med Genet (1994) 0.76
Aortic stiffness with the Williams-Beuren syndrome. Pediatr Cardiol (1997) 0.76
Chromosome abnormalities and Williams-Beuren syndrome. J Med Genet (1993) 0.75
Williams-Beuren syndrome 35 years after the diagnosis in one of the first Beuren patients. Am J Med Genet (2000) 0.75
Magnetic resonance imaging of the brain in Williams-Beuren syndrome. Am J Med Genet (1997) 0.75
Metacarpophalangeal pattern profile (MCPP) analysis in Williams-Beuren Syndrome (WBS). Am J Med Genet (2001) 0.75
[Diastrophic dysplasia. A congenital syndrome with remarkable changes of the external ear and stridor]. HNO (1990) 0.75
How necessary is a chromosomal analysis in growth-retarded girls? Clin Genet (1990) 0.75
Dermatoglyphic peculiarities in patients with Williams-Beuren syndrome. Am J Med Genet (1994) 0.75