15 results on '"Acquila, M."'
Search Results
2. Prenatal diagnosis of haemophilia B: the Italian experience
3. Modified inverse shifting-PCR (IS-PCR) to investigate intron 22 inversion: PO-MO-125
4. Molecular analysis of severe factor XI deficiency in three Italian patients
5. A novel point mutation in severe haemophilia A: a further proof of genotype-phenotype correlation
6. Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand gene
7. An uncommon case of a female carrier of two distinct X-linked disorders
8. MLPA assay in F8 gene mutation screening
9. Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B
10. Identification of mutations in exon 14 including five novelties in 13 Italian patients with haemophilia A
11. Germ-line origin of intron 1 inversion in two haemophilia A families
12. Mutation analysis is an essential strategy in the genetic counselling of sporadic haemophilia B families
13. Detection of somatic mosaicism in sporadic haemophilia B
14. A new strategy for prenatal diagnosis in a sporadic haemophilia B family
15. A novel point mutation in severe haemophilia A: a further proof of genotype-phenotype correlation
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