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Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)

โœ Scribed by Leichtman, Lawrence G. ;Strum, Daniel ;Brothman, Arthur R.


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

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Hunter-McAlpine syndrome is an autosomal dominant disorder consisting of variable manifestations including craniosynostosis, almond-shaped palpebral fissures, small mouth, mild acral-skeletal anomalies, short stature, and mental deficiency. W e report on a 9-year-old boy with this phenotype with mor