Williams-Beuren syndrome (WBS) is a genetic disorder characterized by physical and intellectual developmental delay, associated with congenital heart disease and facial dysmorphism. WBS is caused by a microdeletion on chromosome 7 (7q11.23), which encompasses the elastin (ELN) gene and about 27 other genes. The gold standard for WBS laboratory diagnosis is FISH (fluorescence in situ hybridization), which is very costly. As a possible alternative, we investigated the accuracy of three clinical diagnostic scoring systems in 250 patients with WBS diagnosed by FISH. We concluded that all three systems could be used for the clinical diagnosis of WBS, but they all gave a low percentage of false-positive (6.0-9.2%) and false-negative (0.8-4.0%) re...
Most people with Williams syndrome (WS) have a heterozygous 1.55 Mb deletion on chromosome 7q11.23. ...
Williams-Beuren syndrome (WBS) is clinically characterized by a distinctive "elfin" facial appearan...
Williams-Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion ...
Fil: Leme, D. E. S. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamen...
system for clinical diagnosis. Clinics. 2007:62(2):159-66. OBJECTIVE: To develop a scoring system ba...
Fluorescent in situ hybridization (FISH) with commercial probes covering the elastin gene (ELN) was ...
Williams-Beuren syndrome (WBS) is a genetic disease caused by a microdeletion in the 7q11.23 region....
INTRODUCTION: Williams-Beuren syndrome (WBS; OMIM 194050) is caused by a hemizygous contiguous gene ...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
We have developed a dual probe quantitative PCR (qPCR ) mini array enabling a more accurate analysis...
Abstract Background ...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
OBJECTIVE: To develop and compare two new technologies for diagnosing a contiguous gene syndrome, th...
OBJECTIVE: To develop and compare two new technologies for diagnosing a contiguous gene syndrome, th...
OBJECTIVE: To evaluate the cardiovascular findings and clinical follow-up of patients with Williams-...
Most people with Williams syndrome (WS) have a heterozygous 1.55 Mb deletion on chromosome 7q11.23. ...
Williams-Beuren syndrome (WBS) is clinically characterized by a distinctive "elfin" facial appearan...
Williams-Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion ...
Fil: Leme, D. E. S. Universidade Estadual Paulista. Instituto de Biociencias de Botucatu. Departamen...
system for clinical diagnosis. Clinics. 2007:62(2):159-66. OBJECTIVE: To develop a scoring system ba...
Fluorescent in situ hybridization (FISH) with commercial probes covering the elastin gene (ELN) was ...
Williams-Beuren syndrome (WBS) is a genetic disease caused by a microdeletion in the 7q11.23 region....
INTRODUCTION: Williams-Beuren syndrome (WBS; OMIM 194050) is caused by a hemizygous contiguous gene ...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
We have developed a dual probe quantitative PCR (qPCR ) mini array enabling a more accurate analysis...
Abstract Background ...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
OBJECTIVE: To develop and compare two new technologies for diagnosing a contiguous gene syndrome, th...
OBJECTIVE: To develop and compare two new technologies for diagnosing a contiguous gene syndrome, th...
OBJECTIVE: To evaluate the cardiovascular findings and clinical follow-up of patients with Williams-...
Most people with Williams syndrome (WS) have a heterozygous 1.55 Mb deletion on chromosome 7q11.23. ...
Williams-Beuren syndrome (WBS) is clinically characterized by a distinctive "elfin" facial appearan...
Williams-Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion ...