25 results on '"Fattorini, C."'
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2. PROGNOSTIC ASSESSMENT OF PREGNANCIES AT RISK FOR MYOTONIC-DYSTROPHY BASED ON THE CTG EXPANSION
3. (CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients
4. Focus The dynamic genomics of myotonic dystrophy and its clinical relevance: an overview
5. Expansion of the myotonic dystrophy gene in Italian and Spanish patients.
6. (CTG)nTriplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients
7. Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle
8. Expression of sugars biosynthesis-related genes during fruit ripening in normal and salt-exposed fig plants
9. Expansion of the myotonic dystrophy gene in Italian and Spanish patients
10. LACCASE IN TRICHODERMA VIRENS: ENZYMATIC ACTIVITY AND GENE EXPRESSION IN RESPONSE TO DIFFERENT SUBSTRATES.
11. Development and Validation of MPS-Based System for Human Appearance Prediction in Challenging Forensic Samples
12. Mixed mucinous adenocarcinoma/large cell neuroendocrine carcinoma of the uterine cervix: case report and molecular characterization of a rare entity.
13. HER2-low metastases of HER2-negative primary tumors: a single institution analysis of intertumoral and internodal heterogeneity in node-positive breast cancer.
14. Vascular tree-in-bud sign in Pulmonary Tumour Thrombotic Microangiopathy (PTTM): CT findings for a difficult radiological early antemortem diagnosis.
15. VviAGL11 self-regulates and targets hormone- and secondary metabolism-related genes during seed development.
16. Surgeon-Pathologist Team Approach Dramatically Affects Lymph Nodes Detection and Improves Patients' Short-Term Outcome.
17. The Grape Gene Reference Catalogue as a Standard Resource for Gene Selection and Genetic Improvement.
18. Papillary-cystic neoplasms of the middle ear are distinct from endolymphatic sac tumours.
19. Potential utility of a 4-marker immunohistochemistry panel to predict response to cisplatin-based neoadjuvant chemotherapy in patients with muscle-invasive bladder cancer: a single-center preliminary experience.
20. Behçet disease in Emergency Department: a rare case presenting with haemoptysis and massive pulmonary arterial aneurysms.
21. Moving from qPCR to Chip Digital PCR Assays for Tracking of some Fusarium Species Causing Fusarium Head Blight in Cereals.
22. North Eurasian origin of the myotonic dystrophy mutation.
23. Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle.
24. The dynamic genomics of myotonic dystrophy and its clinical relevance: an overview.
25. Genotyping of spinal muscular atrophy families with linked DNA probes.
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