Heterozygous truncating mutations in the RP1 gene cause approximately 7% of autosomal dominant retinitis pigmentosa (RP) cases. To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for s
โฆ LIBER โฆ
The premaxilla: Embryological evidence that it does not exist in man
โ Scribed by Wood, Norman K. ;Wragg, Laurence E. ;Stuteville, Orion H.
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 308 KB
- Volume
- 158
- Category
- Article
- ISSN
- 0003-276X
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