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
β¦ LIBER β¦
Interstitial Deletion 13q31 Associated with Normal Phenotype: Cytogenetic Study of a Family with Concomitant Segregation of Reciprocal Translocation and Interstitial Deletion
β Scribed by Yu-Yuan Ke; Dong-Jay Lee; Gwo-Chin Ma; Mei-Hui Lee; Bao-Tyan Wang; Ming Chen
- Book ID
- 117630251
- Publisher
- Chinese Electronic Periodical Services
- Year
- 2007
- Tongue
- English
- Weight
- 681 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0929-6646
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