8 results on '"Chetta M"'
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2. A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome
3. Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A
4. Severe outbreaks of polyarthritis in kids caused by Mycoplasma mycoides subspecies capri in Sicily
5. Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency
6. Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH
7. Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A
8. Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization
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