## Abstract [Nguyen et al. (2003); Am J Med Genet 121A: 109–112] reported a boy with severe hypocholesterolemia due to autosomal dominant hypobetalipoproteinemia (ADBHL) associated with severe growth retardation, mental deficiency, epicanthal folds, a short nose with low nasal bridge and anteverted
A familial MCA/MR syndrome due to translocation t(10;16)(q26;p13.1): Report of six cases
✍ Scribed by Bofinger, Mary K. ;Opitz, John M. ;Soukup, Shirley W. ;Ekblom, Linda S. ;Phillips, S. ;Daniel, Arthur ;Greene, Edward W.
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 793 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0148-7299
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