Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay

• Main Authors: Go Hun Seo (Author), Ja Hye Kim (Author), Ja Hyang Cho (Author), Gu-Hwan Kim (Author), Eul-Ju Seo (Author), Beom Hee Lee (Author), Jin-Ho Choi (Author), Han-Wook Yoo (Author)
• Format: Book
• Published: Korean Pediatric Society, 2016-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

PurposeThe 1p36 deletion syndrome is a microdeletion syndrome characterized by developmental delays/intellectual disability, craniofacial dysmorphism, and other congenital anomalies. To date, many cases of this syndrome have been reported worldwide. However, cases with this syndrome have not been re...