Published in Z Kardiol on April 01, 1997
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Mechanical properties of the common carotid artery in Williams syndrome. Heart (2000) 0.94
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Echocardiographic findings in patients with Williams-Beuren syndrome. Wien Klin Wochenschr (2006) 0.84
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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
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
Linguistic abilities in children with Williams-Beuren syndrome. Am J Med Genet (1994) 0.86
Videodensitometric studies by a new method of quantitating the amount of contrast medium. Eur J Cardiol (1974) 0.82
Longitudinal study of the cognitive development in children with Williams-Beuren syndrome. Am J Med Genet (1996) 0.81
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
The spectrum of ocular features in the Williams-Beuren syndrome. Clin Genet (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
Williams-Beuren syndrome and celiac disease. J Pediatr Gastroenterol Nutr (1996) 0.80
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Digital angiography in the diagnosis of congenital heart disease. Cardiovasc Intervent Radiol (1984) 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
Assessment of arterial blood flow measurements by digital angiography. Radiology (1981) 0.78
Diaphragmatic defect in Brachmann-de Lange syndrome: a further observation. Am J Med Genet (1993) 0.77
Aortic stiffness with the Williams-Beuren syndrome. Pediatr Cardiol (1997) 0.76
Use of digitized functional angiography to evaluate arterial blood flow. Cardiovasc Intervent Radiol (1983) 0.76
Hormonal regulation in children and adults with Williams-Beuren syndrome. Am J Med Genet (1994) 0.76
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Hepatic encephalopathy and ascites. Lancet (1998) 0.75
Chromosome abnormalities and Williams-Beuren syndrome. J Med Genet (1993) 0.75
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Magnetic resonance imaging of the brain in Williams-Beuren syndrome. Am J Med Genet (1997) 0.75
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Metacarpophalangeal pattern profile (MCPP) analysis in Williams-Beuren Syndrome (WBS). Am J Med Genet (2001) 0.75