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Article

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

29 Mar 1996

Abstract excerpt

Smith-Magenis syndrome (SMS) is a multiple congenital anomaly, mental retardation (MCA/MR) syndrome associated with deletion of chromosome 17 band p11.2. As part of a multi-disciplinary clinical, cytogenetic, and molecular approach to SMS, detailed clinical studies including radiographic, neurologic, developmental, ophthalmologic, otolaryngologic, and audiologic evaluations were performed on 27 SMS patients....

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Identifiers

PMID: 8882782
DOI: 10.1002/(sici)1096-8628(19960329)62:3<247::aid-ajmg9>3.0.co;2-q

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Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)PMID 8882782Read ↗

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