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Johnson-McMillin syndrome, a neuroectodermal syndrome with conductive hearing loss and microtia: Report of a new case

✍ Scribed by Schweitzer, Daniela N. ;Yano, Shoji ;Earl, Dawn L. ;Graham, John M.

Book ID
111698217
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
111 KB
Volume
120A
Category
Article
ISSN
0148-7299

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## Abstract ## BACKGROUND Johnson‐McMillin syndrome (JMS) is a rare neuroectodermal disorder characterized by alopecia, ear malformations, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism. It is inherited in an autosomal dominant manner; however, the causative gene has