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American Journal of Medical Genetics|August 10, 2001
Association study of a promoter polymorphism of UFD1L gene with schizophreniaA De Luca, A Pasini, F Amati, et al.Molecular Syndromology|December 23, 2011
RASopathies: Clinical Diagnosis in the First Year of LifeM C Digilio, F Lepri, A Baban, et al.Mediators of Inflammation|September 30, 2003
Protein carbonyl group content in patients affected by familiar chronic nail candidiasisS Gangemi, A Saija, A Tomaino, et al.Journal of Medical Genetics|July 5, 2005
Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletionsC Howald, G Merla, M C Digilio, et al.International Journal of Immunopathology and Pharmacology|March 10, 2007
Prolonged remission of neuro-Behcet disease following autologous transplantationA De Cata, D Intiso, M Bernal, et al.Clinical Genetics|September 14, 2017
Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and reviewE Agolini, M L Dentici, E Bellacchio, et al.American Journal of Medical Genetics|November 11, 1996
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeatsM Gennarelli, G Novelli, F Andreasi Bassi, et al.Gene Therapy|June 27, 2001
Expression of DeltaF508 CFTR in normal mouse lung after site-specific modification of CFTR sequences by SFHRK K Goncz, A Colosimo, B Dallapiccola, et al.International Journal of Cancer|April 12, 2021
Systemic toxicities of trastuzumab-emtansine predict tumor response in HER2+ metastatic breast cancerShou-Ching Tang, Carter L Capra, Germame H Ajebo, et al.Disease Markers|May 31, 2001
Evidence for an association between the SRD5A2 (type II steroid 5 alpha-reductase) locus and prostate cancer in Italian patientsK Margiotti, F Sangiuolo, A De Luca, et al.Pageof 34