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1
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)
Bastepe, M., | Elsevier Inc | 2011 ,
2
Patterns of FGF-23, DMP1, and MEPE expression in patients with chronic kidney disease
Patterns of FGF-23, DMP1, and MEPE expression in patients with chronic kidney disease
Pereira, R. C., | Elsevier Inc | 2009 ,
3
Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
Turan, S., | Elsevier Inc | 2010 ,
4
Guided Course in English Composition
Guided Course in English Composition
Jupp, T C., 746-J95g | Heinemann Educational Books | 1981 746-J95g,
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