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- [21] DNA methylation signature associated with Bohring-Opitz syndrome: A new tool for functional classification of variants in ASXL genesEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 178 - 178Awamleh, Zain论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, CanadaChater-Diehl, Eric论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, CanadaChoufani, Sanaa论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, CanadaArboleda, Valerie论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, CanadaRussell, Bianca论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Dept Pediat, Los Angeles, CA USA Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, CanadaWeksberg, Rosanna论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, Canada
- [22] DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genesEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (06) : 695 - 702Awamleh, Zain论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaChater-Diehl, Eric论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaChoufani, Sanaa论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaWei, Elizabeth论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaKianmahd, Rebecca R.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Genet, Los Angeles, CA 90095 USA Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaYu, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Genet, Los Angeles, CA 90095 USA Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaChad, Lauren论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Div Clin & Metab Genet, Toronto, ON, Canada Univ Toronto, Dept Paediat, Toronto, ON, Canada Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada论文数: 引用数: h-index:机构:Tan, Wen-Hann论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaScherer, Stephen W.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada Univ Toronto, Dept Mol Genet, Toronto, ON, Canada Univ Toronto, Inst Med Sci, Toronto, ON, Canada Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaArboleda, Valerie A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Dept Computat Med, Los Angeles, CA USA Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, CanadaRussell, Bianca E.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Genet, Los Angeles, CA 90095 USA Hosp Sick Children, Res Inst, Genet & Genome Biol Program, Toronto, ON, Canada论文数: 引用数: h-index:机构:
- [23] DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genesEuropean Journal of Human Genetics, 2022, 30 : 695 - 702Zain Awamleh论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteEric Chater-Diehl论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteSanaa Choufani论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteElizabeth Wei论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteRebecca R. Kianmahd论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteAnna Yu论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteLauren Chad论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteGregory Costain论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteWen-Hann Tan论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteStephen W. Scherer论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteValerie A. Arboleda论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteBianca E. Russell论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research InstituteRosanna Weksberg论文数: 0 引用数: 0 h-index: 0机构: The Hospital for Sick Children,Genetics and Genome Biology Program, Research Institute
- [24] The ultrarare ASXL-related disorders: two novel cases of Sashi-Pena and Bohring-Opitz syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 469 - 469Contro, Gianluca论文数: 0 引用数: 0 h-index: 0机构: Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, ItalyCaraffi, Stefano论文数: 0 引用数: 0 h-index: 0机构: Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, ItalyRadio, Francesca Clementina论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Bambino Gesu Childrens Hosp, Genet & Rare Dis Res Div, I-00165 Rome, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, ItalyFrattini, Daniele论文数: 0 引用数: 0 h-index: 0机构: Azienda USL IRCCS Reggio Emilia, Dept Pediat, Child Neurol & Psychiat Unit, Reggio Emilia, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, ItalyFusco, Carlo论文数: 0 引用数: 0 h-index: 0机构: Azienda USL IRCCS Reggio Emilia, Dept Pediat, Child Neurol & Psychiat Unit, Reggio Emilia, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, ItalyTartaglia, Marco论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Bambino Gesu Childrens Hosp, Genet & Rare Dis Res Div, I-00165 Rome, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, ItalyGaravelli, Livia论文数: 0 引用数: 0 h-index: 0机构: Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, Italy Azienda USL IRCCS Reggio Emilia, Med Genet Unit, Reggio Emilia, Italy
- [25] Novel truncating recessive mutations in KLHL7 gene causing Bohring-Opitz like syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 479 - 479Bruel, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, France Univ Bourgogne, FHU TRANSLAD, CHU Dijon, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceBigoni, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp St Anna, UOL Med Genet, Dept Reprod & Growth, Ferrara, Italy Univ Hosp St Anna, Dept Med Sci, Ferrara, Italy Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, France论文数: 引用数: h-index:机构:Whiteford, M.论文数: 0 引用数: 0 h-index: 0机构: Queen Elizabeth Univ Hosp, Dept Clin Genet, Glasgow G51 4TF, Lanark, Scotland Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceBuxton, C.论文数: 0 引用数: 0 h-index: 0机构: Southmead Hosp, Bristol Genet Lab, Bristol, Avon, England Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceParmeggiani, G.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp St Anna, UOL Med Genet, Dept Reprod & Growth, Ferrara, Italy Univ Hosp St Anna, Dept Med Sci, Ferrara, Italy Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceWherlock, M.论文数: 0 引用数: 0 h-index: 0机构: Southmead Hosp, Bristol Genet Lab, Bristol, Avon, England Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceWoodward, G.论文数: 0 引用数: 0 h-index: 0机构: Southmead Hosp, Bristol Genet Lab, Bristol, Avon, England Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceGreenslade, M.论文数: 0 引用数: 0 h-index: 0机构: Southmead Hosp, Bristol Genet Lab, Bristol, Avon, England Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceWilliams, M.论文数: 0 引用数: 0 h-index: 0机构: Southmead Hosp, Bristol Genet Lab, Bristol, Avon, England Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceSt-Onge, J.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Ctr Hlth, Dept Human Genet, RI MUHC, Montreal, PQ, Canada Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceFerlini, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp St Anna, Neonatal Intens Care Unit, Dept Reprod & Growth, Ferrara, Italy Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceGarani, G.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp St Anna, Neonatal Intens Care Unit, Dept Reprod & Growth, Ferrara, Italy Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceBallardini, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp St Anna, Neonatal Intens Care Unit, Dept Reprod & Growth, Ferrara, Italy Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceGilissen, C.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, Francevan Bon, B.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceAcuna-Hildago, R.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceBorhing, A.论文数: 0 引用数: 0 h-index: 0机构: Westfalische Wilhelms Univ, Inst Humangenet, Munster, Germany Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceRiviere, J.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Ctr Hlth, Dept Human Genet, RI MUHC, Montreal, PQ, Canada Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceBrunner, H. G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceHoischen, A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceNewbury-Ecob, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp NHS Fdn trust, Clin Genet Dept, St Michaels Hosp, Bristol BS2 8EG, Avon, England Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceThauvin-Robinet, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, France Univ Bourgogne, FHU TRANSLAD, CHU Dijon, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceFaivre, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, France Univ Bourgogne, FHU TRANSLAD, CHU Dijon, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, FranceThevenon, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, France Univ Bourgogne, FHU TRANSLAD, CHU Dijon, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR 1231, GAD Team,Genet Dev Disorders, Dijon, France
- [26] ASXL1 mutations are frequent in de novo AML with trisomy 8 and confer an unfavorable prognosisLEUKEMIA & LYMPHOMA, 2017, 58 (01) : 204 - 206Zong, Xiangping论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaYao, Hong论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaWen, Lijun论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaMa, Liang论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaWang, Qinrong论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaYang, Zhiluo论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaZhang, Tongtong论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaChen, Suning论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R ChinaWu Depei论文数: 0 引用数: 0 h-index: 0机构: Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China Soochow Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Thrombosis & Hemostasis,Jiangsu Inst Hema, 188 Shizi St, Suzhou 215006, Peoples R China
- [27] ASXL1 Mutations Associated with Cytogenetic Findings in DE NOVO and Secondary Acute Myeloid LeukemiaANNALS OF HEMATOLOGY, 2015, 94 : S80 - S80Kakosaiou, K.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreeceDaraki, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreeceApostolou, P.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Sci Res Demokritos, Mol Diagnost Lab, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreeceZachaki, S.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreecePagoni, M.论文数: 0 引用数: 0 h-index: 0机构: Evangelismos Med Ctr, Dept Hematol & Lymphoma, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreeceSambani, C.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreeceDimitriadis, G.论文数: 0 引用数: 0 h-index: 0机构: Univ Gen Hosp Attikon, Med Sch Athens, Hematol Unit, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreecePapa, V.论文数: 0 引用数: 0 h-index: 0机构: Univ Gen Hosp Attikon, Med Sch Athens, Hematol Unit, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, GreeceManola, K. N.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, Greece Natl Ctr Sci Res Demokritos, Lab Hlth Phys Radiobiol & Cytogenet, Athens, Greece
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- [29] A de novo truncating mutation in ASXL1 associated with segmental overgrowthJournal of Genetics, 2019, 98Stephanie Efthymiou论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of NeurologyVincenzo Salpietro论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of NeurologyErica Pironti论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of NeurologyMaria Bonsignore论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of NeurologyValentina Ferrazzoli论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of NeurologyGabriella Di Rosa论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of NeurologyHenry Houlden论文数: 0 引用数: 0 h-index: 0机构: University College London,Department of Neuromuscular Disorders, Institute of Neurology
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