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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1984
[A case of Flaiani-Basedow-Graves disease]B Colombo, F Cogliati, P Morelli, et al.Clinical Genetics|November 27, 1998
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutationS Russo, V Briscioli, F Cogliati, 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.Clinical Dysmorphology|August 24, 2000
Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1 biallelic expressionS Russo, M F Bedeschi, F Cogliati, et al.American Journal of Medical Genetics|October 26, 2000
Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian familyS Russo, F Cogliati, F Cavalleri, et al.Human Mutation|March 29, 2000
Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndromeS Russo, F Cogliati, M Viri, et al.Neurogenetics|February 26, 2009
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypesS Russo, M Marchi, F Cogliati, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1993
[Celiac disease and the evolution of its diagnosis. Comparison and experience at a hospital pediatric department (1975-1993). (Second part)]M A Della Morte, M R Sala, P Morelli, et al.Diagnostic Microbiology and Infectious Disease|February 27, 2021
Determinants of prolonged viral RNA shedding in hospitalized patients with SARS-CoV-2 infectionF Cogliati Dezza, A Oliva, F Cancelli, et al.Journal of Medical Genetics|August 3, 2006
Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann regionS Russo, P Finelli, M P Recalcati, et al.Pageof 2