✦ LIBER ✦
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells
✍ Scribed by Helen A Mintz-Hittner; Elena V Semina; Laura J Frishman; Thomas C Prager; Jeffrey C Murray
- Book ID
- 116802775
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- English
- Weight
- 623 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0161-6420
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