부산대학교 도서관

Hoang HD; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Spillmann RC; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, 905 Lasalle Street, Durham, NC 27710, United States.; Wegner DJ; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Tedesco MG; Medical Genetics and Rare Diseases Unit, Maternal-Infantile Department, Hospital of Perugia, Piazzale Menghini 8/9, 06129 Perugia, Italy.; Brohus M; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.; Novelli A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Viale San Paolo 15, 00146 Rome, Italy.; Stregapede F; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Viale San Paolo 15, 00146 Rome, Italy.; Rogaia D; Medical Genetics and Rare Diseases Unit, Maternal-Infantile Department, Hospital of Perugia, Piazzale Menghini 8/9, 06129 Perugia, Italy.; Troiani S; Neonatal Intensive Care Unit, Maternal-Infantile Department, Hospital of Perugia, Piazzale Menghini 1, 06129 Perugia, Italy.; Lesinski J; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Yuan W; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Fielder SM; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Zhang B; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Morrison S; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Regmi S; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Foti MRS; Genetics Unit, Medical Science and Maternal-Infantile Department, Hospital Sant'Anna of Ferrara, Via Fossato di Mortara, 74, 44121 Ferrara, Italy.; Baldridge D; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Silverman GA; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Shea P; Institute for Genome Medicine, Columbia University Medical Center, 630 West 168th Street, New York, NY 10032, United States.; Dickson P; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Wambach JA; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Overgaard MT; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.; Jensen HH; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.; Olsen A; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.; Prontera P; Medical Genetics and Rare Diseases Unit, Maternal-Infantile Department, Hospital of Perugia, Piazzale Menghini 8/9, 06129 Perugia, Italy.; Shashi V; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, 905 Lasalle Street, Durham, NC 27710, United States.; Pak SC; Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, United States.; Schedl T; Department of Genetics, Washington University in St. Louis School of Medicine, 4523 Clayton Ave St. Louis, MO 63110, United States.

Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

Prontera P; Rogaia D; Sallicandro E; Mencarelli A; Imperatore V; Squeo GM; Merla G; Elisei S; Moretti-Ferreira D; Esposito S; Stangoni G

European Journal of Human Genetics. 27:1260-1266

Ruggeri, Loredana; Capanni, Marusca; Urbani, Elena; Perruccio, Katia; Shlomchik, Warren D.; Tosti, Antonella; Posati, Sabrina; Rogaia, Daniela; Frassoni, Francesco; Aversa, Franco; Martelli, Massimo F.; Velardi, Andrea

Science, 2002 Mar . 295(5562), 2097-2100.

Prontera P; Ottaviani V; Rogaia D; Isidori I; Mencarelli A; Malerba N; Cocciadiferro D; Rolph P; Stangoni G; Vulto-vanSilfhout A; Merla G

American Journal of Medical Genetics. Part A, 170, 9, pp. 2377-82

Prontera P; Napolioni V; Ottaviani V; Rogaia D; Fusco C; Augello B; Serino D; Parisi V; Bernardini L; Merla G; Cavanna AE; Donti E

neurogenetics. 15:237-242

Foti MRS; Unità di Genetica Medica, Azienda Ospedaliera Sant'Anna, Dip. Scienze Mediche e Dip. Materno-Infantile, 44121 Ferrara, Italy.; Tedesco MG; Istituto Malattie Rare 'Mauro Baschirotto', Costozza di Longare, 36100 Vicenza, Italy.; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Colavito D; Research & Innovation (R&I Genetics) Srl, 35100 Padova, Italy.; Rogaia D; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Mencarelli A; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Schippa M; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Gradassi C; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Romani R; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Department of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.; Ardisia C; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.; Prontera P; UOSD Genetica Medica e Malattie Rare, Dip. Materno-Infantile, Azienda Ospedaliera di Perugia, 06129 Perugia, Italy.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

Grignani Fr.; Testa U.; Rogaia D.; Ferrucci P. F.; Samoggia P.; Pinto A.; Aldinucci D.; Gelmetti V.; Fagioli M.; Alcalay M.; Seeler J.; Grignani F.; Nicoletti I.; Peschle C.; Pelicci P. G.

The EMBO Journal. 15:4949-4958

Farnè M; Medical Genetics Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.; Medical Genetics Unit, Department of Medical Sciences, Ferrara University Hospital, Italy.; Tedesco GM; Medical Genetics Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.; Clinical Genetics Unit, Department of Women and Children's Health, University of Padova, Padova, Italy.; Genetics Unit, 'Mauro Baschirotto' Institute for Rare Diseases (B.I.R.D.), Costozza di Longare, Vicenza, Italy.; Bedetti C; Istituto Serafico Assisi, Perugia, Italy.; Mencarelli A; Medical Genetics Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.; Rogaia D; Medical Genetics Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.; Colavito D; Research&Innovation Srl, Padova, Italy.; Di Cara G; Pediatric Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.; Stangoni G; Medical Genetics Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.; Troiani S; Division of Neonatology and Neonatal Intensive Care Unit, Santa Maria della Misericordia Hospital of Perugia, Perugia, Italy.; Ferlini A; Medical Genetics Unit, Department of Medical Sciences, Ferrara University Hospital, Italy.; Prontera P; Medical Genetics Unit, Santa Maria della Misericordia Hospital, University of Perugia, Perugia, Italy.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Flex E; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.; Imperatore V; Medical Genetics Unit, University and Hospital of Perugia, 06129 Perugia, Italy.; Carpentieri G; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.; Bruselles A; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.; Ciolfi A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.; Pizzi S; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.; Tedesco MG; Medical Genetics Unit, University and Hospital of Perugia, 06129 Perugia, Italy.; Rogaia D; Medical Genetics Unit, University and Hospital of Perugia, 06129 Perugia, Italy.; Mencarelli A; Medical Genetics Unit, University and Hospital of Perugia, 06129 Perugia, Italy.; Di Cara G; Pediatric Clinic, University and Hospital of Perugia, 06129 Perugia, Italy.; Verrotti A; Pediatric Clinic, University and Hospital of Perugia, 06129 Perugia, Italy.; Troiani S; Neonatal Intensive Care Unit, University and Hospital of Perugia, 06129 Perugia, Italy.; Merla G; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy.; Tartaglia M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.; Prontera P; Medical Genetics Unit, University and Hospital of Perugia, 06129 Perugia, Italy.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

Tedesco MG; Medical Genetics Unit, Santa Maria della Misericordia Hospital and University of Perugia, Perugia, Italy.; Genetics Unit, 'Mauro Baschirotto' Institute for Rare Diseases (B.I.R.D.), Vicenza, Italy.; Lonardo F; Medical Genetics Unit, 'San Pio' Hospital, Benevento, Italy.; Ceccarini C; Cytogenetics Unit, Policlinico Riuniti, University Hospitals Foggia, Foggia, Italy.; Cesarano C; Cytogenetics Unit, Policlinico Riuniti, University Hospitals Foggia, Foggia, Italy.; Digilio MC; Laboratory of Medical Genetics, Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Magliozzi M; Laboratory of Medical Genetics, Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Rogaia D; Medical Genetics Unit, Santa Maria della Misericordia Hospital and University of Perugia, Perugia, Italy.; Mencarelli A; Medical Genetics Unit, Santa Maria della Misericordia Hospital and University of Perugia, Perugia, Italy.; Leoni C; Department of Woman and Child Health and Public Health, Center for Rare Diseases and Birth Defects, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Piscopo C; U.O.S.C. Medical Genetics, A.O.R.N. 'A. Cardarelli', Naples, Italy.; Imperatore V; Medical Genetics Unit, Santa Maria della Misericordia Hospital and University of Perugia, Perugia, Italy.; Falco MT; Medical Genetics Unit, 'San Pio' Hospital, Benevento, Italy.; Fontana P; Medical Genetics Unit, 'San Pio' Hospital, Benevento, Italy.; Nardone AM; Medical Genetics Laboratory, 'Policlinico Tor Vergata' Hospital, Rome, Italy.; Novelli A; Laboratory of Medical Genetics, Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Troiani S; Medical Genetics Unit, Santa Maria della Misericordia Hospital and University of Perugia, Perugia, Italy.; Division of Neonatology and Neonatal Intensive Care Unit, Santa Maria della Misericordia Hospital of Perugia, Perugia, Italy.; Seri M; Medical Genetics Unit, Policlinico S. Orsola-Malpighi, University of Bologna, Bologna, Italy.; Prontera P; Medical Genetics Unit, Santa Maria della Misericordia Hospital and University of Perugia, Perugia, Italy.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Testa, U; Grignani, F; Hassan, HJ; Rogaia, D; Masciulli, R; Gelmetti, V; Guerriero, R; Macioce, G; Liberatore, C; Barberi, T; Mariani, G; Pelicci, PG; Peschle, C

Leukemia. 12(4):563-570

PRONTERA P; BERNARDINI L; STANGONI G; CAPALBO A; ROGAIA D; ARDISIA C; NOVELLI A; DALLA PICCOLA B; DONTI, Emilio

Rooney K; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada.; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.; Levy MA; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.; Haghshenas S; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada.; Kerkhof J; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.; Rogaia D; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.; Tedesco MG; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.; Imperatore V; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.; Mencarelli A; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.; Squeo GM; Laboratory of Regulatory and Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.; Di Venere E; Laboratory of Regulatory and Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.; Di Cara G; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.; Verrotti A; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.; Merla G; Laboratory of Regulatory and Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80100 Naples, Italy.; Tedder ML; Greenwood Genetic Center, Greenwood, SC 29646, USA.; DuPont BR; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Sadikovic B; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada.; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.; Prontera P; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

Prontera, P.; Buldrini, B.; Aiello, V.; Rogaia, D.; Mencarelli, A.; Gruppioni, R.; Bonfatti, A.; Beltrami, N.; Donti, E.; Sensi, A.

GENETIC COUNSELING; 2010, 21 1, p91-p97, 7p.

Prontera, P.; Ferraando, B.; Giuliani, V.; Falcinelli, F.; Mencarelli, A.; Rogaia, D.; Pasini, B.; Donti, E.

GENETIC COUNSELING; 2008, 19 4, p413-p418, 6p.

Prontera P; Centro di Riferimento Regionale di Genetica Medica, Azienda Ospedaliera-Universitaria di Perugia, Perugia, Italy.; Ottaviani V; Toccaceli D; Rogaia D; Ardisia C; Romani R; Stangoni G; Pierini A; Donti E

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Allanson J; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada. allanson@cheo.on.ca; Smith A; Hare H; Albrecht B; Bijlsma E; Dallapiccola B; Donti E; Fitzpatrick D; Isidor B; Lachlan K; Le Caignec C; Prontera P; Raas-Rothschild A; Rogaia D; van Bon B; Aradhya S; Crocker SF; Jarinova O; McGowan-Jordan J; Boycott K; Bulman D; Fagerberg CR

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Grignani, F; Gelmetti, V; Fanelli, M; Rogaia, D; De Matteis, S; Ferrara, FF; Bonci, D; Nervi, C; Pelicci, PG

ONCOGENE; NOV 4 1999, 18 46, p6313-p6321, 9p.

Prontera P; Medical Genetics Unit, University of Perugia, Perugia, Italy ; Department of Experimental Medicine and Biochemical Sciences, University of Perugia, Perugia, Italy.; Bartocci A; Ottaviani V; Isidori I; Rogaia D; Ardisia C; Guercini G; Mencarelli A; Donti E

Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

Prontera, P.; Le Caignec, C.; Philippe, J.; Martin-Coignard, D.; Gunn, C. S.; Lindenbaum, P.; Bokobza, C.; Redon, R.; Sallicandro, E.; Mencarelli, A.; Rogaia, D.; Gradassi, C.; Schippa, M.; Romani, R.; Ardisia, C.; Merla, G.; Troiani, S.; Stangoni, G.; Davis, E. E.

EUROPEAN JOURNAL OF HUMAN GENETICS; JUL 2019, 27 p782-p782, 1p. Supplement: 1