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- [31] ANKRD11突变导致KBG综合征1例江苏医药, 2022, 48 (03) : 320 - 322王朝论文数: 0 引用数: 0 h-index: 0机构: 南京中医药大学附属医院儿科叶进论文数: 0 引用数: 0 h-index: 0机构: 南京中医药大学附属医院儿科
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Marseille, France CHU Rouen, Serv Genet, Rouen, FranceCacciagli, Pierre论文数: 0 引用数: 0 h-index: 0机构: Aix Marseille Univ, INSERM, GMGF, Marseille, France CHU Rouen, Serv Genet, Rouen, FranceCapri, Yline论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, Unite Fonct Genet Clin, Paris, France CHU Rouen, Serv Genet, Rouen, France论文数: 引用数: h-index:机构:Delahaye-Duriez, Andree论文数: 0 引用数: 0 h-index: 0机构: CHU Paris Seine St Denis, Hop Jean Verdier, AP HP, Lab Histol Embryol Cytogenet BDR, Bondy, France Univ Paris 13, Sorbonne Paris Cite, Bondy, France CHU Rouen, Serv Genet, Rouen, France论文数: 引用数: h-index:机构:Gatinois, Vincent论文数: 0 引用数: 0 h-index: 0机构: CHRU Montpellier, Hop Arnaud Villeneuve, Lab Genet Malad Rares & Autoinflammatoires, Montpellier, France CHU Rouen, Serv Genet, Rouen, FranceGuerrot, Anne-Marie论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, France Univ Rouen, U1079, INSERM, Rouen, France Ctr Normand Genom Med & Med Personnalisee, Rouen, France CHU Rouen, Serv Genet, Rouen, FranceGenevieve, David论文数: 0 引用数: 0 h-index: 0机构: CHRU Montpellier, Hop Arnaud Villeneuve, Dept Genet Med, Montpellier, France CHU Rouen, Serv Genet, Rouen, France论文数: 引用数: h-index:机构:Jacquette, Aurelia论文数: 0 引用数: 0 h-index: 0机构: Grp Hosp Pitie Salpetriere, APHP,Dept Genet, Ctr Reference Deficiences Intellectuelles Causes, GRC UPMC Deficiences Intellectuelles & Autisme, Paris, France CHU Rouen, Serv Genet, Rouen, FranceVan Kien, Philippe Khau论文数: 0 引用数: 0 h-index: 0机构: CHU Nimes, Hop Caremeau, Unite Fonct Genet Med & Cytogenet, Nimes, France CHU Rouen, Serv Genet, Rouen, FranceLeheup, Bruno论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Hop Brabois, Serv Genet Clin, Nancy, France CHU Rouen, Serv Genet, Rouen, FranceMarlin, Sandrine论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Serv Genet, Paris, France CHU Rouen, Serv Genet, Rouen, FranceVerloes, Alain论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, Unite Fonct Genet Clin, Paris, France CHU Rouen, Serv Genet, Rouen, FranceMichaud, Vincent论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, GH Pellegrin, Serv Genet Med, Bordeaux, France CHU Rouen, Serv Genet, Rouen, FranceNadeau, Gwenael论文数: 0 引用数: 0 h-index: 0机构: CH Valence, Unite Fonct Cytogenet, Valence, France CHU Rouen, Serv Genet, Rouen, FranceMignot, Cyril论文数: 0 引用数: 0 h-index: 0机构: Grp Hosp Pitie Salpetriere, APHP,Dept Genet, Ctr Reference Deficiences Intellectuelles Causes, GRC UPMC Deficiences Intellectuelles & Autisme, Paris, France CHU Rouen, Serv Genet, Rouen, FranceParent, Philippe论文数: 0 引用数: 0 h-index: 0机构: CHRU Brest, Hop Morvan, Dept Pediat & Genet Med, Brest, France CHU Rouen, Serv Genet, Rouen, FranceRossi, Massimiliano论文数: 0 引用数: 0 h-index: 0机构: CHU Lyon, GH Est, Hop Femme Mere Enfant, Serv Genet, Lyon, France CHU Rouen, Serv Genet, Rouen, FranceToutain, Annick论文数: 0 引用数: 0 h-index: 0机构: CHRU Tours, Hop Bretonneau, Serv Genet, Tours, France CHU Rouen, Serv Genet, Rouen, FranceSchaefer, Elise论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, FranceThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, FranceVan Maldergem, Lionel论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, FranceThevenon, Julien论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, FranceSatre, Veronique论文数: 0 引用数: 0 h-index: 0机构: Univ Grenoble Alpes, Unite Fonct Genet Chromosom, Hop Couple Enfant, CHU Grenoble,INSERM 1209,CNRS,UMR 5309, Grenoble, France CHU Rouen, Serv Genet, Rouen, FrancePerrin, Laurence论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, Unite Fonct Genet Clin, Paris, France CHU Rouen, Serv Genet, Rouen, FranceVincent-Delorme, Catherine论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, FranceSorlin, Arthur论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Hop Brabois, Serv Genet Clin, Nancy, France CHU Rouen, Serv Genet, Rouen, FranceMissirian, Chantal论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants La Timone, AP HP, Dept Genet Med, Marseille, France CHU Rouen, Serv Genet, Rouen, FranceVillard, Laurent论文数: 0 引用数: 0 h-index: 0机构: Aix Marseille Univ, INSERM, GMGF, Marseille, France CHU Rouen, Serv Genet, Rouen, FranceMancini, Julien论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Serv Genet, Rouen, France论文数: 引用数: h-index:机构:Philip, Nicole论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants La Timone, AP HP, Dept Genet Med, Marseille, France Aix Marseille Univ, INSERM, GMGF, Marseille, France CHU Rouen, Serv Genet, Rouen, France
- [33] Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG SyndromeINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (11)论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Tumiatti, Francesca论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyMasciadri, Maura论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalySmeland, Marie Falkenberg论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp North Norway, Dept Med Genet, N-9019 Tromso, Norway IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyNaik, Swati论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, Clin Genet Unit, Birmingham B15 2TG, W Midlands, England IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyMurch, Oliver论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Wales, All Wales Med Genom Serv, Cardiff CF14 4XW, Wales IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyBonati, Maria Teresa论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, San Luca Hosp, Clin Med Genet, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalySpano, Alice论文数: 0 引用数: 0 h-index: 0机构: Fdn MBBM, San Gerardo Hosp, Clin Pediat Genet Unit, Pediat Clin, I-20900 Monza, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyCattaneo, Elisa论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, V Buzzi Childrens Hosp, Dept Obstet & Gynecol, Clin Genet Unit, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyMariani, Milena论文数: 0 引用数: 0 h-index: 0机构: ASST Lariana, Pediat Unit, I-22100 Como, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyGotta, Fabio论文数: 0 引用数: 0 h-index: 0机构: ASST Cremona, Clin Genet, Via Concordia 1, I-26100 Cremona, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyCrosti, Francesca论文数: 0 引用数: 0 h-index: 0机构: S Gerardo Hosp, Clin Pathol Dept, Med Genet Lab, I-20900 Monza, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyCavalli, Pietro论文数: 0 引用数: 0 h-index: 0机构: ASST Cremona, Clin Genet, Via Concordia 1, I-26100 Cremona, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyPantaleoni, Chiara论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol Carlo Besta, Dept Pediat Neurosci, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyNatacci, Federica论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Genet Unit, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyBedeschi, Maria Francesca论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Genet Unit, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyMilani, Donatella论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Pediat Highly Intens Care, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyMaitz, Silvia论文数: 0 引用数: 0 h-index: 0机构: Fdn MBBM, San Gerardo Hosp, Clin Pediat Genet Unit, Pediat Clin, I-20900 Monza, Italy Oncol Inst Southern Switzerland, Serv Med Genet, EOC, CH-6900 Lugano, Switzerland IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalySelicorni, Angelo论文数: 0 引用数: 0 h-index: 0机构: ASST Lariana, Pediat Unit, I-22100 Como, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalySpaccini, Luigina论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, V Buzzi Childrens Hosp, Dept Obstet & Gynecol, Clin Genet Unit, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyPeron, Angela论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, San Paolo Hosp, Child Neuropsychiat Unit Epilepsy Ctr, Dept Hlth Sci,ASST Santi Paolo & Carlo, I-20142 Milan, Italy ASST Santi Paolo & Carlo, Med Genet, San Paolo Hosp, I-20142 Milan, Italy Univ Utah, Dept Pediat, Div Med Genet, Sch Med, Salt Lake City, UT 84132 USA IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyRusso, Silvia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, ItalyLarizza, Lidia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, Italy IRCCS Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, I-20142 Milan, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [34] Further delineation of the KBG syndrome caused by ANKRD11 aberrations (vol 23, pg 1176, 2015)EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (09) : 1270 - 1270Ockeloen, Charlotte W.论文数: 0 引用数: 0 h-index: 0Willemsen, Marjolein H.论文数: 0 引用数: 0 h-index: 0de Munnik, Sonja论文数: 0 引用数: 0 h-index: 0van Bon, Bregje W. M.论文数: 0 引用数: 0 h-index: 0de Leeuw, Nicole论文数: 0 引用数: 0 h-index: 0Verrips, Aad论文数: 0 引用数: 0 h-index: 0Kant, Sarina G.论文数: 0 引用数: 0 h-index: 0Jones, Elizabeth A.论文数: 0 引用数: 0 h-index: 0Brunner, Han G.论文数: 0 引用数: 0 h-index: 0van Loon, Rosa L. E.论文数: 0 引用数: 0 h-index: 0Smeets, Eric E. J.论文数: 0 引用数: 0 h-index: 0van Haelst, Mieke M.论文数: 0 引用数: 0 h-index: 0van Haaften, Gijs论文数: 0 引用数: 0 h-index: 0Nordgren, Ann论文数: 0 引用数: 0 h-index: 0Malmgren, Helena论文数: 0 引用数: 0 h-index: 0Grigelioniene, Giedre论文数: 0 引用数: 0 h-index: 0Vermeer, Sascha论文数: 0 引用数: 0 h-index: 0Louro, Pedro论文数: 0 引用数: 0 h-index: 0Ramos, Lina论文数: 0 引用数: 0 h-index: 0Maal, Thomas J. J.论文数: 0 引用数: 0 h-index: 0van Heumen, Celeste C.论文数: 0 引用数: 0 h-index: 0Yntema, Helger G.论文数: 0 引用数: 0 h-index: 0Carels, Carine E. L.论文数: 0 引用数: 0 h-index: 0Kleefstra, Tjitske论文数: 0 引用数: 0 h-index: 0
- [35] Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 444 - 445de Boer, Elke论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Donders Inst, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsOckeloen, Charlotte论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsKampen, Rosalie A.论文数: 0 引用数: 0 h-index: 0机构: MPI Psycholinguist, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsHampstead, Juliet论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands RIMLS, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsDingemans, Alexander论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Donders Inst, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsRots, Dmitrijs论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Donders Inst, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsAshraf, Tazeen论文数: 0 引用数: 0 h-index: 0机构: Great Ormond Str Hosp Children NHS, London, England Guys & St Thomas NHS, London, England Radboudumc, Human Genet, Nijmegen, NetherlandsBaker, Rachel论文数: 0 引用数: 0 h-index: 0机构: Advocate Childrens Hosp, Park Ridge, IL USA Radboudumc, Human Genet, Nijmegen, NetherlandsBarat-Houari, Mouna论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Montpellier, France Radboudumc, Human Genet, Nijmegen, NetherlandsAngle, Brad论文数: 0 引用数: 0 h-index: 0机构: Advocate Childrens Hosp, Park Ridge, IL USA Radboudumc, Human Genet, Nijmegen, NetherlandsChatron, Nicolas论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Lyon, France Inst NeuroMyoGene, Lyon, France Radboudumc, Human Genet, Nijmegen, NetherlandsDenomme-Pichon, Anne-Sophie论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Dijon, France Lab Genet Chromosom & Mol, Dijon, France Radboudumc, Human Genet, Nijmegen, NetherlandsDevinsky, Orrin论文数: 0 引用数: 0 h-index: 0机构: NYU Grossman Sch Med, New York, NY USA Radboudumc, Human Genet, Nijmegen, NetherlandsDubourg, Christele论文数: 0 引用数: 0 h-index: 0机构: Serv Genet Mol & Genom, Rennes, France Univ Rennes, Rennes, France Radboudumc, Human Genet, Nijmegen, NetherlandsElmslie, Frances论文数: 0 引用数: 0 h-index: 0机构: St Georges, London, England Radboudumc, Human Genet, Nijmegen, NetherlandsMonaghan, Kristin论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Radboudumc, Human Genet, Nijmegen, NetherlandsElloumi, Houda论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Radboudumc, Human Genet, Nijmegen, NetherlandsFaivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: Ctr Genet, Dijon, France Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Federat Hosp Univ Med TRANS LAD, Dijon, France Radboudumc, Human Genet, Nijmegen, NetherlandsFitzgerald-Butt, Sara论文数: 0 引用数: 0 h-index: 0机构: Indiana Univ, 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Radboudumc, Human Genet, Nijmegen, NetherlandsOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Rennes, France Radboudumc, Human Genet, Nijmegen, NetherlandsPfundt, Rolph论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsPutoux, Audrey论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Lyon, France Ctr Rech Neurosci Lyon, Lyon, France Radboudumc, Human Genet, Nijmegen, Netherlandsvan Reeuwijk, Jeroen论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Donders Inst, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsSanten, Gijs论文数: 0 引用数: 0 h-index: 0机构: Leiden UMC, Leiden, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsSasaki, Erina论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, NetherlandsSorlin, Arthur论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Dijon, France Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Radboudumc, Human Genet, Nijmegen, Netherlandsvan der Spek, Peter论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, NetherlandsStegmann, Alexander论文数: 0 引用数: 0 h-index: 0机构: Maastricht UMC, AzM, Maastricht, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsSwagemakers, Sigrid论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, NetherlandsViora-Dupont, Eleonore论文数: 0 引用数: 0 h-index: 0机构: Ctr Genet, Dijon, France Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Radboudumc, Human Genet, Nijmegen, NetherlandsVitobello, Antonio论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Dijon, France Lab Genet Chromosom & Mol, Dijon, France Radboudumc, Human Genet, Nijmegen, Netherlands论文数: 引用数: h-index:机构:Weber, Mathys论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, NetherlandsGilissen, Christian论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands RIMLS, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsLow, Karen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bristol, Weston NHS, Bristol, England Radboudumc, Human Genet, Nijmegen, NetherlandsFisher, Simon论文数: 0 引用数: 0 h-index: 0机构: MPI Psycholinguist, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsVissers, Lisenka论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Donders Inst, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsWong, Maggie论文数: 0 引用数: 0 h-index: 0机构: MPI Psycholinguist, Nijmegen, Netherlands Radboudumc, Human Genet, Nijmegen, NetherlandsKleefstra, Tjitske论文数: 0 引用数: 0 h-index: 0机构: Radboudumc, Human Genet, Nijmegen, Netherlands Donders Inst, Nijmegen, Netherlands Vincent van Gogh Inst, Venray, Netherlands Radboudumc, Human Genet, Nijmegen, Netherlands
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