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Confirmation of a particular but nonspecific metacarpophalangeal pattern profile in patients with the Smith-Magenis syndrome due to interstitial deletion of 17p

✍ Scribed by Meinecke, Peter


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
364 KB
Volume
45
Category
Article
ISSN
0148-7299

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## Abstract Smith–Magenis syndrome (SMS) is a disorder characterized by multiple congenital anomalies and behavior problems, including abnormal sleep patterns. It is most commonly due to a 3.5 Mb interstitial deletion of chromosome 17 band p11.2. Secretion of melatonin, a hormone produced by the pi