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- [1] The 2q23.1 microdeletion syndrome: clinical and behavioural phenotypeEuropean Journal of Human Genetics, 2010, 18 : 163 - 170Bregje WM van Bon论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsDavid A Koolen论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsLouise Brueton论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsDominic McMullan论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsKlaske D Lichtenbelt论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsLesley C Adès论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsGregory Peters论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsKate Gibson论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsFrancesca Novara论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsTiziano Pramparo论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsBernardo Dalla Bernardina论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsLeonardo Zoccante论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsUmberto Balottin论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsFausta Piazza论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsVanna Pecile论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsPaolo Gasparini论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsVeronica Guerci论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsMarleen Kets论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsRolph Pfundt论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsArjan P de Brouwer论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsJoris A Veltman论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsNicole de Leeuw论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsMeredith Wilson论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsJayne Antony论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsSantina Reitano论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsDaniela Luciano论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsMarco Fichera论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsCorrado Romano论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsHan G Brunner论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsOrsetta Zuffardi论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsBert BA de Vries论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human Genetics
- [2] The 2q23.1 microdeletion syndrome: clinical and behavioural phenotypeEUROPEAN JOURNAL OF HUMAN GENETICS, 2010, 18 (02) : 163 - 170van Bon, Bregje W. M.论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKoolen, David A.论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Univ Birmingham, Div Med & Mol Genet, Birmingham, W Midlands, England RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsBrueton, Louise论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Div Med & Mol Genet, Birmingham, W Midlands, England RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsMcMullan, Dominic论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsLichtenbelt, Klaske D.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsAdes, Lesley C.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsPeters, Gregory论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsGibson, Kate论文数: 0 引用数: 0 h-index: 0机构: Royal Brisbane & Womens Hosp, Brisbane, Qld, Australia RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands论文数: 引用数: h-index:机构:Pramparo, Tiziano论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, I-27100 Pavia, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsDalla Bernardina, Bernardo论文数: 0 引用数: 0 h-index: 0机构: Univ Verona, Child Neuropsychiat Unit, Policlin GB Rossi, I-37100 Verona, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Piazza, Fausta论文数: 0 引用数: 0 h-index: 0机构: Univ Verona, Child Neuropsychiat Unit, Policlin GB Rossi, I-37100 Verona, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsPecile, Vanna论文数: 0 引用数: 0 h-index: 0机构: IRCCS Burlo Garafano, Cytogenet Lab, Trieste, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands论文数: 引用数: h-index:机构:Guerci, Veronica论文数: 0 引用数: 0 h-index: 0机构: Univ Trieste, IRCCS Burlo Garofolo, Trieste, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKets, Marleen论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsPfundt, Rolph论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsde Brouwer, Arjan P.论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsVeltman, Joris A.论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsde Leeuw, Nicole论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsWilson, Meredith论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsAntony, Jayne论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsReitano, Santina论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsLuciano, Daniela论文数: 0 引用数: 0 h-index: 0机构: IRCCS Assoc Oasi Maria Santissima, Lab Genet Diag, Troina, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsFichera, Marco论文数: 0 引用数: 0 h-index: 0机构: IRCCS Assoc Oasi Maria Santissima, Lab Genet Diag, Troina, Italy RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsRomano, Corrado论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsBrunner, Han G.论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands论文数: 引用数: h-index:机构:de Vries, Bert B. A.论文数: 0 引用数: 0 h-index: 0机构: RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands RUNMC, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
- [3] Correction: Corrigendum to: The 2q23.1 microdeletion syndrome: clinical and behavioural phenotypeEuropean Journal of Human Genetics, 2010, 18 (2) : 170 - 170Bregje WM van Bon论文数: 0 引用数: 0 h-index: 0David A Koolen论文数: 0 引用数: 0 h-index: 0Louise Brueton论文数: 0 引用数: 0 h-index: 0Dominic McMullan论文数: 0 引用数: 0 h-index: 0Klaske D Lichtenbelt论文数: 0 引用数: 0 h-index: 0Lesley C Adès论文数: 0 引用数: 0 h-index: 0Gregory Peters论文数: 0 引用数: 0 h-index: 0Kate Gibson论文数: 0 引用数: 0 h-index: 0Francesca Novara论文数: 0 引用数: 0 h-index: 0Tiziano Pramparo论文数: 0 引用数: 0 h-index: 0Bernardo Dalla Bernardina论文数: 0 引用数: 0 h-index: 0Leonardo Zoccante论文数: 0 引用数: 0 h-index: 0Umberto Balottin论文数: 0 引用数: 0 h-index: 0Fausta Piazza论文数: 0 引用数: 0 h-index: 0Vanna Pecile论文数: 0 引用数: 0 h-index: 0Paolo Gasparini论文数: 0 引用数: 0 h-index: 0Veronica Guerci论文数: 0 引用数: 0 h-index: 0Marleen Kets论文数: 0 引用数: 0 h-index: 0Rolph Pfundt论文数: 0 引用数: 0 h-index: 0Arjan P de Brouwer论文数: 0 引用数: 0 h-index: 0Joris A Veltman论文数: 0 引用数: 0 h-index: 0Nicole de Leeuw论文数: 0 引用数: 0 h-index: 0Meredith Wilson论文数: 0 引用数: 0 h-index: 0Jayne Antony论文数: 0 引用数: 0 h-index: 0Santina Reitano论文数: 0 引用数: 0 h-index: 0Daniela Luciano论文数: 0 引用数: 0 h-index: 0Marco Fichera论文数: 0 引用数: 0 h-index: 0Corrado Romano论文数: 0 引用数: 0 h-index: 0Han G Brunner论文数: 0 引用数: 0 h-index: 0Orsetta Zuffardi论文数: 0 引用数: 0 h-index: 0Bert BA de Vries论文数: 0 引用数: 0 h-index: 0
- [4] The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype (vol 18, pg 163, 2010)EUROPEAN JOURNAL OF HUMAN GENETICS, 2010, 18 (10) : 1171 - 1171Van Bon, Bregje W. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyKoolen, David A.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyBrueton, Louise论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyMcMullan, Dominic论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyLichtenbelt, Klaske D.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyAdes, Lesley C.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyPeters, Gregory论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyGibson, Kate论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyMoloney, Susan论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyNovara, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyPramparo, Tiziano论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyDalla Bernardina, Bernardo论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyZoccante, Leonardo论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, Italy论文数: 引用数: h-index:机构:Piazza, Fausta论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, Italy Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyPecile, Vanna论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyGasparini, Paolo论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyGuerci, Veronica论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyKets, Marleen论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyPfundt, Rolph论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, Italyde Brouwer, Arjan P.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyVeltman, Joris A.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, Italyde Leeuw, Nicole论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyWilson, Meredith论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyAntony, Jayne论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyReitano, Santina论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyLuciano, Daniela论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyFichera, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyRomano, Corrado论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyBrunner, Han G.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, ItalyZuffardi, Orsetta论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, Italyde Vries, Bert B. A.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Child & Neuropsychiat Unit, IRCCS Fdn C Mondino, I-27100 Pavia, Italy
- [5] Microdeletion 2q23.1 and syndromic findingsREVISTA DE NEUROLOGIA, 2013, 57 (09) : 430 - 431Perez-Gay, Laura论文数: 0 引用数: 0 h-index: 0机构: Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, SpainGomez-Lado, Carmen论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Fac Med, Hosp Clin Univ, Dept Pediat,Serv Neuropediat, Santiago De Compostela, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, SpainEiris-Punal, Jesus论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Fac Med, Hosp Clin Univ, Dept Pediat,Serv Neuropediat, Santiago De Compostela, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, SpainDacruz, David论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Fac Med, Hosp Clin Univ, Dept Pediat,Serv Neuropediat, Santiago De Compostela, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, SpainQuintela, Ines论文数: 0 引用数: 0 h-index: 0机构: Fdn Publ Galega Med Xenom, Santiago De Compostela, A Coruna, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, SpainBarros-Angueira, Francisco论文数: 0 引用数: 0 h-index: 0机构: Fdn Publ Galega Med Xenom, Santiago De Compostela, A Coruna, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, SpainCastro-Gago, Manuel论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Fac Med, Hosp Clin Univ, Dept Pediat,Serv Neuropediat, Santiago De Compostela, Spain Hosp Clin Univ Lucus Augusti, Serv Pediat, Lugo, Spain
- [6] Trapping MBD5 to understand 2q23.1 microdeletion syndromeEMBO MOLECULAR MEDICINE, 2014, 6 (08) : 993 - 994Kwon, Deborah Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Genet, Perelman Sch Med, Philadelphia, PA 19104 USA Univ Penn, Dept Genet, Perelman Sch Med, Philadelphia, PA 19104 USAZhou, Zhaolan论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Genet, Perelman Sch Med, Philadelphia, PA 19104 USA Univ Penn, Dept Genet, Perelman Sch Med, Philadelphia, PA 19104 USA
- [7] Cytogenetically pseudobalanced chromosome 2 structural rearrangements associated with 2q23.1 microdeletion syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 983 - 983Kolotii, A. D.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaVorsanova, S. G.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaYurov, Y. B.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaKurinnaia, O. S.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaZelenova, M. A.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaBulatnikova, M. A.论文数: 0 引用数: 0 h-index: 0机构: Stem Cell Bank Pokrovsky, St Petersburg, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaIourov, I. Y.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia FSBEI FPE Russian Med Acad Postgrad Educ, Minist Healthcare Russian Federat, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia
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- [9] Neurodevelopmental Features in 2q23.1 Microdeletion Syndrome: Report of a New Patient With Intractable Seizures and Review of LiteratureAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (04) : 861 - 868Motobayashi, Mitsuo论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanNishimura-Tadaki, Akira论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanInaba, Yuji论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanKosho, Tomoki论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Med Genet, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanMiyatake, Satoko论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanNiimi, Taemi论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanNishimura, Takafumi论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanWakui, Keiko论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Med Genet, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanFukushima, Yoshimitsu论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Med Genet, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanMatsumoto, Naomichi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, JapanKoike, Kenichi论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Dept Pediat, Sch Med, Matsumoto, Nagano 3908621, Japan
- [10] Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndromeEMBO MOLECULAR MEDICINE, 2014, 6 (08) : 1003 - 1015Camarena, Vladimir论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USACao, Lei论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAAbad, Clemer论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAAbrams, Alexander论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAToledo, Yaima论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAAraki, Kimi论文数: 0 引用数: 0 h-index: 0机构: Kumamoto Univ, Inst Resource Dev & Anal, Kumamoto, Japan Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAAraki, Masatake论文数: 0 引用数: 0 h-index: 0机构: Kumamoto Univ, Inst Resource Dev & Anal, Kumamoto, Japan Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAWalz, Katherina论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USAYoung, Juan I.论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Dept Human Genet, John T Macdonald Fdn, Miami, FL USA