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Gynecologic and Obstetric Investigation|January 1, 1996
Expression pattern of c-sis, c-fos and c-jun in human placenta and embryofetal organsD Rossi, L Del Giacco, L Doneda, et al.Cancer Genetics and Cytogenetics|October 23, 1997
Cytogenetic study of pituitary adenomasD Bettio, N Rizzi, D Giardino, et al.American Journal of Medical Genetics|February 22, 2002
Pure 6p22-pter trisomic patient: refined FISH characterization and genotype-phenotype correlationD Giardino, P Finelli, D Caufin, et al.Human Molecular Genetics|September 26, 2000
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemiaA Beghini, C B Ripamonti, P Peterlongo, et al.American Journal of Medical Genetics|March 17, 2001
Refined FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndromeP Finelli, D Giardino, S Russo, et al.American Journal of Medical Genetics|March 27, 1995
FISH analysis in Prader-Willi and Angelman syndrome patientsD Bettio, N Rizzi, D Giardino, et al.Clinical Genetics|October 1, 1996
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failureP Riva, I Magnani, A M Fuhrmann Conti, et al.American Journal of Medical Genetics|January 9, 2001
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotypeF Natacci, L Corrado, M Pierri, et al.International Journal of Cancer|April 13, 2000
Non-random trisomies of chromosomes 5, 8 and 12 in the prolactinoma sub-type of pituitary adenomas: conventional cytogenetics and interphase FISH studyP Finelli, D Giardino, N Rizzi, et al.Cancer|August 16, 2001
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosaA Beghini, M G Tibiletti, G Roversi, et al.Pageof 11