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- [21] Relation between phosphatase activity of SHP2 mutants and phenotype in Noonan/LEOPARD syndromeEUROPEAN HEART JOURNAL, 2006, 27 : 810 - 810Narita, J.论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Pediat, Osaka, JapanKogaki, S.论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Pediat, Osaka, JapanNasuno, S.论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Pediat, Osaka, JapanTakahashi, K.论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Pediat, Osaka, JapanNamba, N.论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Pediat, Osaka, JapanOzono, K.论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Pediat, Osaka, Japan
- [22] Different Role Of Shp2 Mutants In Cardiomyocyte Hypertrophy In Noonan/leopard Syndrome SpectrumCIRCULATION, 2008, 118 (18) : S333 - S333Narita, Jun论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanKogaki, Shigetoyo论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanIshida, Hidekazu论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanIchimori, Hiroaki论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanUchikawa, Toshiki论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanNasuno, Sayaka论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanOkada, Yoko论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanYoshida, Yoko论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, JapanOzono, Kelichi论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch, Osaka, Japan Osaka Univ, Grad Sch, Osaka, Japan
- [23] Noonan and LEOPARD syndrome Shp2 variants induce heart displacement defects in zebrafishDEVELOPMENT, 2014, 141 (09): : 1961 - 1970Bonetti, Monica论文数: 0 引用数: 0 h-index: 0机构: Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands Univ Med Ctr Utrecht, NL-3584 CT Utrecht, Netherlands Hubrecht Inst KNAW, NL-3584 CT Utrecht, NetherlandsOverman, Jeroen Paardekooper论文数: 0 引用数: 0 h-index: 0机构: Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands Univ Med Ctr Utrecht, NL-3584 CT Utrecht, Netherlands Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands论文数: 引用数: h-index:机构:Noel, Emily论文数: 0 引用数: 0 h-index: 0机构: Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands Univ Med Ctr Utrecht, NL-3584 CT Utrecht, Netherlands Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands论文数: 引用数: h-index:机构:den Hertog, Jeroen论文数: 0 引用数: 0 h-index: 0机构: Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands Univ Med Ctr Utrecht, NL-3584 CT Utrecht, Netherlands Inst Biol, NL-2333 CC Leiden, Netherlands Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands
- [24] Visual Processing in Noonan Syndrome: Dorsal and Ventral Stream SensitivityAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (10) : 2459 - 2464Alfieri, Paolo论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyCesarini, Laura论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ, Pediat Neurol Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyDe Rose, Paola论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyRicci, Daniela论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ, Pediat Neurol Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalySelicorni, Angelo论文数: 0 引用数: 0 h-index: 0机构: Fdn MBBM, AO San Gerardo, Monza, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyMenghini, Deny论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyGuzzetta, Andrea论文数: 0 引用数: 0 h-index: 0机构: Sci Inst Stella Maris, Dept Dev Neurosci, Pisa, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyBaranello, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ, Pediat Neurol Unit, Rome, Italy Ist Nazl Neurol Carlo Besta, Dev Neurol Unit, Milan, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyTinelli, Francesca论文数: 0 引用数: 0 h-index: 0机构: Sci Inst Stella Maris, Dept Dev Neurosci, Pisa, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyMallardi, Maria论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ, Pediat Neurol Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyZampino, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ, Serv Epidemiol, Rome, Italy Catholic Univ, Clin Difetti Congeniti Ist Clin Pediat, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyVicari, Stefano论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyAtkinson, Janette论文数: 0 引用数: 0 h-index: 0机构: UCL, Dept Psychol, Visual Dev Unit, London, England Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, ItalyMercuri, Eugenio论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ, Pediat Neurol Unit, Rome, Italy Childrens Hosp, Dept Neurosci, Child Neuropsychiat Unit, Rome, Italy
- [25] Abnormalities of pubertal development and gonadal function in Noonan syndromeFRONTIERS IN ENDOCRINOLOGY, 2023, 14Patti, Giuseppa论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyScaglione, Marco论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyMaiorano, Nadia Gabriella论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyRosti, Giulia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Clin Genet & Genom, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyDivizia, Maria Teresa论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Clin Genet & Genom, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyCamia, Tiziana论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyDe Rose, Elena Lucia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyZucconi, Alice论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyCasalini, Emilio论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyNapoli, Flavia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyDi Iorgi, Natascia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, ItalyMaghnie, Mohamad论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Dept Pediat, Genoa, Italy
- [26] GENITAL-TRACT FUNCTION IN MEN WITH NOONAN SYNDROMEJOURNAL OF MEDICAL GENETICS, 1994, 31 (06) : 468 - 470ELSAWI, MM论文数: 0 引用数: 0 h-index: 0机构: UNIV LONDON KINGS COLL,LONDON SE5 9PJ,ENGLANDPRYOR, JP论文数: 0 引用数: 0 h-index: 0机构: UNIV LONDON KINGS COLL,LONDON SE5 9PJ,ENGLANDKLUFIO, G论文数: 0 引用数: 0 h-index: 0机构: UNIV LONDON KINGS COLL,LONDON SE5 9PJ,ENGLANDBARNES, C论文数: 0 引用数: 0 h-index: 0机构: UNIV LONDON KINGS COLL,LONDON SE5 9PJ,ENGLANDPATTON, MA论文数: 0 引用数: 0 h-index: 0机构: UNIV LONDON KINGS COLL,LONDON SE5 9PJ,ENGLAND
- [27] Craniofacial and cutaneous findings in Noonan, Costello and LEOPARD syndromesPOSTEPY DERMATOLOGII I ALERGOLOGII, 2018, 35 (05): : 437 - 441Pokrowiecki, Rafal论文数: 0 引用数: 0 h-index: 0机构: Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, Poland Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, PolandChomik, Piotr论文数: 0 引用数: 0 h-index: 0机构: Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, Poland Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, PolandBorowiec, Maciej论文数: 0 引用数: 0 h-index: 0机构: Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, Poland Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, PolandDowgierd, Krzysztof论文数: 0 引用数: 0 h-index: 0机构: Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, Poland Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, PolandStarzynska, Anna论文数: 0 引用数: 0 h-index: 0机构: Med Univ Gdansk, Dept Oral Surg, Gdansk, Poland Voivodeship Specialist Childrens Hosp, Dept Maxillofacial Surg, 7 Debinki St, PL-80952 Olsztyn, Poland
- [28] Genetic heterogeneity in the multiple lentigines/LEOPARD/Noonan syndromesAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 127A (03) : 324 - 326Pacheco, TR论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Dept Dermatol & Cutaneous Oncol, Denver, CO 80262 USAOreskovich, N论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Dept Dermatol & Cutaneous Oncol, Denver, CO 80262 USAFain, P论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Hlth Sci Ctr, Dept Dermatol & Cutaneous Oncol, Denver, CO 80262 USA
- [29] Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyNATURE GENETICS, 2007, 39 (08) : 1007 - 1012Pandit, Bhaswati论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USASarkozy, Anna论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAPennacchio, Len A.论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USACarta, Claudio论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAOishi, Kimihiko论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAMartinelli, Simone论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAPogna, Edgar A.论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USASchackwitz, Wendy论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAUstaszewska, Anna论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USALandstrom, Andrew论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USABos, J. Martijn论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAOmmen, Steve R.论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAEsposito, Giorgia论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USALepri, Francesca论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAFaul, Christian论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAMundel, Peter论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USASiguero, Juan P. Lopez论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USATenconi, Romano论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USASelicorni, Angelo论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USARossi, Cesare论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAMazzanti, Laura论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USATorrente, Isabella论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAMarino, Bruno论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USADigilio, Maria C.论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAZampino, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAAckerman, Michael J.论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USADallapiccola, Bruno论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USATartaglia, Marco论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USAGelb, Bruce D.论文数: 0 引用数: 0 h-index: 0机构: CUNY Mt Sinai Sch Med, Dept Pediat, Ctr Mol Cardiol, New York, NY 10029 USA
- [30] Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyNature Genetics, 2007, 39 : 1007 - 1012Bhaswati Pandit论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesAnna Sarkozy论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesLen A Pennacchio论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesClaudio Carta论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesKimihiko Oishi论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesSimone Martinelli论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesEdgar A Pogna论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesWendy Schackwitz论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesAnna Ustaszewska论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesAndrew Landstrom论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesJ Martijn Bos论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesSteve R Ommen论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesGiorgia Esposito论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesFrancesca Lepri论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesChristian Faul论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesPeter Mundel论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesJuan P López Siguero论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesRomano Tenconi论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesAngelo Selicorni论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesCesare Rossi论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesLaura Mazzanti论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesIsabella Torrente论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesBruno Marino论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesMaria C Digilio论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesGiuseppe Zampino论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesMichael J Ackerman论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesBruno Dallapiccola论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesMarco Tartaglia论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic SciencesBruce D Gelb论文数: 0 引用数: 0 h-index: 0机构: Center for Molecular Cardiology,Department of Pediatrics and Department of Genetics and Genomic Sciences