Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis

[1] Broder K(1999)Elevated ambulatory blood pressure in 20 subjects with Williams syndrome Am J Med Genet 83 356-360

[2] Reinhardt E(1999)Williams-Beuren syndrome: an update and review for the primary physician Clin Pediatr (Phila) 38 189-208

[3] Ahern J(2010)Williams-Beuren syndrome N Engl J Med 362 239-252

[4] Lifton R(2018)Cardiovascular disease in Williams syndrome Curr Opin Pediatr 30 609-615

[5] Tamborlane W(2017)Congenital heart defects in Williams syndrome Turk J Pediatr 59 225-232

[6] Pober B(1988)Natural history of Williams syndrome: physical characteristics J Pediatr 113 318-326

[7] Lashkari A(2018)Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome Ann Hum Genet 82 469-476

[8] Smith AK(2016)162: Prenatal diagnostic testing for genetic disorders Obstet Gynecol 127 e108-e122

[9] Graham JJ(2020)Intrauterine phenotype features of fetuses with Williams-Beuren syndrome and literature review Ann Hum Genet 84 169-176

[10] Pober BR(2019)Prenatal diagnosis of BACs-on-beads assay in 3647 cases of amniotic fluid cells Reprod Sci 26 1005-1012

[1] Broder K(1999)Elevated ambulatory blood pressure in 20 subjects with Williams syndrome Am J Med Genet 83 356-360

[2] Reinhardt E(1999)Williams-Beuren syndrome: an update and review for the primary physician Clin Pediatr (Phila) 38 189-208

[3] Ahern J(2010)Williams-Beuren syndrome N Engl J Med 362 239-252

[4] Lifton R(2018)Cardiovascular disease in Williams syndrome Curr Opin Pediatr 30 609-615

[5] Tamborlane W(2017)Congenital heart defects in Williams syndrome Turk J Pediatr 59 225-232

[6] Pober B(1988)Natural history of Williams syndrome: physical characteristics J Pediatr 113 318-326

[7] Lashkari A(2018)Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome Ann Hum Genet 82 469-476

[8] Smith AK(2016)162: Prenatal diagnostic testing for genetic disorders Obstet Gynecol 127 e108-e122

[9] Graham JJ(2020)Intrauterine phenotype features of fetuses with Williams-Beuren syndrome and literature review Ann Hum Genet 84 169-176

[10] Pober BR(2019)Prenatal diagnosis of BACs-on-beads assay in 3647 cases of amniotic fluid cells Reprod Sci 26 1005-1012