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1. The Past Contribution and Future Fate of Genetic Variants under Climate Change in an Island Population of Musa itinerans.

2. A new variant of the ectodysplasin A receptor death domain gene associated with anhidrotic ectodermal dysplasia in a Turkish family and its simple diagnosis by restriction fragment length polymorphism.

3. Investigation of Genetic Mutations in the Exon-Intron Regions of the COL7A1 Gene in five Family Case Reports with Epidermolysis Bullosa in Khuzestan Province.

4. Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

5. Echocardiography of Marfan's Syndrome Patient with New Gene Mutation of FBN1 with 13-year Follow-up

6. Association of emergence of new mutations in circulating tumuor DNA during chemotherapy with clinical outcome in metastatic colorectal cancer

7. Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations.

8. Clan genomics: From OMIM phenotypic traits to genes and biology.

9. Wiskott-Aldrich Syndrome

10. Wiskott-Aldrich Syndrome: Description of a New Gene Mutation With Normal Platelet Volume.

11. A Novel Mutation (p.Met1?) of a Cuban Patient in the NAGLU Gene with Mucopolysaccharidosis IIIB

12. New Missense Mutation Gly238Ala in the TBX5 Gene and Its Phenotypical Characteristics.

13. Association of emergence of new mutations in circulating tumuor DNA during chemotherapy with clinical outcome in metastatic colorectal cancer.

14. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease.

15. A Homozygous Missense Variant in HSD17B4 Identified in Two Different Families.

16. Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1

17. Meningioma in a patient with Werner syndrome.

19. Repetitive Suicidal Behaviors in a Case With a New Mutation of Wolfram Syndrome: A Jump From the Gene to the Behavior

20. Is the Next Generation Sequencing the Essential Tool for the Early Diagnostic Approach in Congenital Muscular Dystrophy? New Mutation in the Gen LMNA Associated with Serious Phenotype.

21. A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literature

22. A new MEFV gene mutation in an Iranian patient with familial Mediterranean fever

23. Mental retardation, seizures and language delay caused by new SETD1B mutations: Three case reports.

24. Transient liver injury and severe neonatal cholestasis in infant with glucose-6-phosphate dehydrogenase deficiency due to a new mutation.

25. Treating TRAPS Syndrome with a Previously Undescribed TNF α Gene Receptor Mutation Successfully with Canakinumab

26. Emergence of lesions outside of the basal ganglia and irreversible damage to the basal ganglia with severe β-ketothiolase deficiency: A case report

27. X-chromosomale Entwicklungsstörungen im weiblichen Geschlecht.

28. Identification of a Novel Gene Mutation in a Chinese Pedigree with X-linked Thrombocytopenia.

29. A Novel Splice Site Mutation of the ATM Gene Associated with Ataxia Telangiectasia.

30. Myoclonus epilepsy, retinitis pigmentosa, leukoencephalopathy and cerebral calcifications associated with a novel m.5513G>A mutation in the MT-TW gene.

31. Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I

32. Differential evolution with quasi-reflection-based mutation

33. AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution

34. MutTMPredictor: Robust and accurate cascade XGBoost classifier for prediction of mutations in transmembrane proteins

35. A Hybrid Deep Grouping Algorithm for Large Scale Global Optimization

36. RESISTANCE TO THYROID HORMONES: A NOVEL MUTATION OF THE THYROID HORMONE RECEPTOR _ GENE IN AN ALGERIAN FAMILY.

37. A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literature.

38. Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.

39. Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation.

40. A new mutation in the mitochondrial tRNAPro gene associated with early-onset neuromuscular phenotype and ragged-red fibers.

41. Endodontic treatment of dentin dysplasia type I D

42. Implantation of cardiac defibrillator in an infant with hypertrophic cardiomyopathy and newly identified MYBP3 mutation

43. SMBFL: slice-based cost reduction of mutation-based fault localization

44. A Rare Case of Mainly Unilateral Focal Dermal Hypoplasia (Goltz Syndrome) in an Adult Male: A Case Report and Review of the Literature

45. A new mutation affecting the converter region of the beta-myosin heavy chain related to hypertrophic cardiomyopathy with poor prognosis

46. A New Mutation in the MC1R Gene Leads to Unique Carnelian Color in Kurilian Bobtails

48. An Imatinib–non‐responsive patient with an ABL Leu387Trp mutation achieves cytogenetic and molecular response under bosutinib: Case report and biological characterization

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