Learn more 1p36 deletion syndrome (monosomy 1p36 syndrome) is characterized by a deletion on the short arm of chromosome 1.
The disorder is characterized by dysmorphic craniofacial features, developmental delay, brain abnormalities, short feet, severe congenital heart defects, hypotonia, and brachy-/camptodactyly. Learn more Both Angelman (AS), a maternal deletion, and Prader-Willi (PWS), a paternal deletion, syndromes are caused by deletions on the long arm of chromosome 15. The American College of Obstetricians and Gynecologists Committee on Genetics and the Society for Maternal-Fetal Medicine Publications Committee.
This will perform an ajax call to redeem a promotion or gift card and display an informative message upon return.
*/ A.declarative('redeem Promo Code', 'click', function(event) ); /* UTILITY FUNCTIONS show Promos In Popover Render a list if promotions that will be applied to this purchase in the popover below the input box for redeeming a claim code.
Unfortunately, it's not possible to add a specific message to the conversation.