Williams syndrome (WS), also known as Williams–Beuren syndrome (WBS), is a
rare neurodevelopmental disorder characterized by: a distinctive, "elfin" facial ...
Williams syndrome (WS) is a genetic condition that is present at birth and can
affect anyone. It is characterized by medical problems, including cardiovascular ...
Williams syndrome is a developmental disorder that affects many parts of the
body. This condition is characterized by mild to moderate intellectual disability or
Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic
disorder characterized by growth delays before and after birth (prenatal and ...
Jun 9, 2011 ... Williams Syndrome is a rare genetic condition -- so rare, in fact, that few people
have ever heard of it. Of about 7500 newborns, only one will ...
194050 - WILLIAMS-BEUREN SYNDROME; WBS - CHROMOSOME 7q11.23
DELETION SYNDROME, 1.5- TO 1.8-MB;; WILLIAMS SYNDROME; WMS; WS.
Aug 4, 2015 ... Williams syndrome, also called Williams-Beuren syndrome, is a rare genetic
disorder that causes multiple developmental problems. This can ...
Jan 14, 2015 ... Originally described independently by Williams and Beuren in 1961, Williams
syndrome (WS) is a rare genetic condition. The clinical ...
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Information on Williams syndrome, a condition that causes developmental delays
and medical problems throughout the body. Learn the causes, symptoms, ...