Gropman, Andrea L

Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2). [electronic resource] - Pediatric neurology May 2006 - 337-50 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Intramural; Review

0887-8994

10.1016/j.pediatrneurol.2005.08.018 doi


Abnormalities, Multiple--diagnosis
Child
Chromosome Deletion
Chromosomes, Human, Pair 17
Humans
Intellectual Disability--diagnosis
Syndrome