## Abstract Craniometaphyseal dysplasia is caused by mutations in __ANKH__ (ankylosis, progressive homolog [mouse]) in the majority of cases, and all of the reported mutations are single amino acid changes. Genomic DNA from an affected patient, his biological parents, and a sibling was amplified an
Granular cell tumor in a PHTS patient with a novel germlinePTEN mutation
โ Scribed by Marchese, Cristiana ;Montera, Mariapina ;Torrini, Margherita ;Forni, Marco ;Goldoni, Francesca ;Locatelli, Luigi ;Mareni, Cristina
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 145 KB
- Volume
- 120A
- Category
- Article
- ISSN
- 0148-7299
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