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- [21] Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 geneActa Neurologica Belgica, 2015, 115 : 779 - 782Debopam Samanta论文数: 0 引用数: 0 h-index: 0机构: University of Arkansas for Medical Sciences,Division of Child NeurologyErin Willis论文数: 0 引用数: 0 h-index: 0机构: University of Arkansas for Medical Sciences,Division of Child Neurology
- [22] Identification of a novel frameshift variation in ANKRD11: a case report of KBG syndromeFRONTIERS IN GENETICS, 2025, 15Shao, Qing论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaJiang, Qiang论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaLuo, Yuqi论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaMeng, Yimei论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaTian, Guoyu论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaYin, Xiao论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China
- [23] Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 geneACTA NEUROLOGICA BELGICA, 2015, 115 (04) : 779 - 782Samanta, Debopam论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USAWillis, Erin论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USA
- [24] Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndromeMolecular Cytogenetics, 8Milena Crippa论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabDaniela Rusconi论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabChiara Castronovo论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabIlaria Bestetti论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabSilvia Russo论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabAnna Cereda论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabAngelo Selicorni论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabLidia Larizza论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics LabPalma Finelli论文数: 0 引用数: 0 h-index: 0机构: IRCCS Istituto Auxologico Italiano,Medical Cytogenetics and Molecular Genetics Lab
- [25] Clinical and Molecular Findings in 39 Patients with KBG Syndrome Caused by Deletion or Mutation of ANKRD11AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (11) : 2847 - 2859Goldenberg, Alice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, FranceRiccardi, Florence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, FranceTessier, Aude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, FrancePfundt, Rolph论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Afdeling Genet, Nijmegen, Netherlands CHU Rouen, Serv Genet, Rouen, FranceBusa, Tiffany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, 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
- [26] Clinical and molecular findings in three Albanian families with KBG syndrome caused by mutation of ANKRD11 geneEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 237 - 237Babameto-Laku, Anila论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ctr Mother Teresa, Serv Med Genet, Fac Med, Tirana, Albania Univ Hosp Ctr Mother Teresa, Serv Med Genet, Fac Med, Tirana, AlbaniaBushati, Aida论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ctr Mother Teresa, Serv Pediat Neurol, Fac Med, Tirana, Albania Univ Hosp Ctr Mother Teresa, Serv Med Genet, Fac Med, Tirana, AlbaniaGjikopulli, Agim论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ctr Mother Teresa, Serv Pediat Endocrinol, Tirana, Albania Univ Hosp Ctr Mother Teresa, Serv Med Genet, Fac Med, Tirana, Albania
- [27] De novo ANKRD11 and KDM1A gene mutations in a male with features of KBG syndrome and Kabuki syndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (07) : 1744 - 1749Tunovic, Sanjin论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USA Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94158 USA Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USABarkovich, James论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Radiol & Biomol Imaging, San Francisco, CA 94158 USA Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USASherr, Elliott H.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94158 USA Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94158 USA Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USA Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USASlavotinek, Anne M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USA Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94158 USA Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94158 USA
- [28] 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:
- [29] ANKRD11 binding to cohesin suggests a connection between KBG syndrome and Cornelia de Lange syndromePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2025, 122 (04)Liu, Haiyang论文数: 0 引用数: 0 h-index: 0机构: Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R China Shenzhen Bay Lab, Greater Bay Biomed Innocenter, Shenzhen 518036, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaLi, Hao论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Sch Basic Med, Dept Pathophysiol, Wuhan 430030, Peoples R China Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan 430030, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaCai, Qixu论文数: 0 引用数: 0 h-index: 0机构: Xiamen Univ, Sch Publ Hlth, Dept Lab Med, State Key Lab Vaccines Infect Dis, Xiamen 361102, Fujian, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaZhang, Jie论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, State Key Lab Resp Dis, Guangzhou 510530, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaZhong, Hongxin论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, State Key Lab Resp Dis, Guangzhou 510530, Peoples R China Guangzhou Natl Lab, Guangzhou 510005, Peoples R China Univ Chinese Acad Sci, Beijing 100049, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaHu, Gongcheng论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Natl Lab, Guangzhou 510005, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaZhao, Shuaizhu论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Sch Basic Med, Dept Pathophysiol, Wuhan 430030, Peoples R China Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan 430030, Peoples R China Huazhong Univ Sci & Technol, Inst Brain Res, Collaborat Innovat Ctr Brain Sci, Wuhan 430030, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaLu, Yuli论文数: 0 引用数: 0 h-index: 0机构: Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R China Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, State Key Lab Resp Dis, Guangzhou 510530, Peoples R China Univ Chinese Acad Sci, Beijing 100049, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaMao, Yudi论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Bay Lab, Greater Bay Biomed Innocenter, Shenzhen 518036, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaLu, Youming论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Sch Basic Med, Dept Pathophysiol, Wuhan 430030, Peoples R China Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan 430030, Peoples R China Huazhong Univ Sci & Technol, Inst Brain Res, Collaborat Innovat Ctr Brain Sci, Wuhan 430030, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaYao, Hongjie论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Natl Lab, Guangzhou 510005, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R ChinaZhang, Mingjie论文数: 0 引用数: 0 h-index: 0机构: Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R China Shenzhen Bay Lab, Greater Bay Biomed Innocenter, Shenzhen 518036, Peoples R China Southern Univ Sci & Technol, Sch Life Sci, Dept Neurosci, Shenzhen Key Lab Biomol Assembling & Regulat, Shenzhen 518055, Peoples R China
- [30] Enostosis in a patient with KBG syndrome caused by a novel missense ANKRD11 variantCLINICAL DYSMORPHOLOGY, 2022, 31 (03) : 153 - 156Geckinli, Bilgen Bilge论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Yildirim, Ozlem论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Inst Sci, Dept Mol Biol & Genet, Istanbul, Turkey Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, TurkeyArman, Ahmet论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey