Holoprosencephaly is a developmental field defect manifested by a spectrum of abnormalities of the forebrain and midface. Approximately 50% of holoprosencephaly cases are associated with a cytogenetic abnormality or a monogenic syndrome. Suggested risk factors for the remaining 50% of cases have bee
β¦ LIBER β¦
Study of rheumatoid factor in a normal population
β Scribed by Marion Waller; Elam C. Toone
- Publisher
- John Wiley and Sons
- Year
- 1964
- Tongue
- English
- Weight
- 434 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
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