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- [1] Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomasNEURO-ONCOLOGY, 2020, 22 (01) : 128 - 138Surun, Aurore论文数: 0 引用数: 0 h-index: 0机构: SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, France Paris Descartes Univ, Sorbonne Paris Cite, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceVarlet, Pascale论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Univ, Sorbonne Paris Cite, Paris, France St Anne Hosp, Dept Neuropathol, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, France论文数: 引用数: h-index:机构:Lacour, Brigitte论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Univ, INSERM, CRESS Equipe 7, UMRS 1153, Paris, France Nancy Univ Hosp, Natl Registry Solid Tumors, Vandoeuvre Les Nancy, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceFaure-Conter, Cecile论文数: 0 引用数: 0 h-index: 0机构: Ctr Leon Berard, Pediat Hematooncol Inst IHOP, Lyon, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceLeblond, Pierre论文数: 0 引用数: 0 h-index: 0机构: Ctr Oscar Lambret, Pediat Oncol Dept, Lille, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceBertozzi-Salomon, Anne-Isabelle论文数: 0 引用数: 0 h-index: 0机构: Toulouse Univ Hosp, Dept Pathol, Toulouse, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceBerger, Claire论文数: 0 引用数: 0 h-index: 0机构: St Etienne Univ Hosp, Pediat Hematooncol Dept, St Etienne, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceAndre, Nicolas论文数: 0 引用数: 0 h-index: 0机构: Aix Marseille Univ, La Timone, AP HM, Pediat Hematooncol Dept, Marseille, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceSariban, Eric论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, Unite Canc, Brussels, Belgium SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceRaimbault, Sandra论文数: 0 引用数: 0 h-index: 0机构: Paris Saclay Univ, Dept Pediat & Adolescent Oncol, Gustave Roussy Canc Ctr, Villejuif, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FrancePrieur, Fabienne论文数: 0 引用数: 0 h-index: 0机构: St Etienne Univ Hosp, Genet Dept, St Etienne, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceDesseigne, Francoise论文数: 0 引用数: 0 h-index: 0机构: Ctr Leon Berard, Dept Med Oncol, Lyon, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceZattara, Helene论文数: 0 引用数: 0 h-index: 0机构: Marseille Univ, La Timone, Genet Dept, Marseille, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceGuimbaud, Rosine论文数: 0 引用数: 0 h-index: 0机构: Ctr Claudius Regaud, Oncogenet Dept, Toulouse, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FrancePolivka, Marc论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Lariboisiere, Dept Pathol, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceDelisle, Marie-Bernadette论文数: 0 引用数: 0 h-index: 0机构: Toulouse Univ Hosp, Dept Pathol, Toulouse, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceVasiljevic, Alexandre论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Dept Pathol, Lyon, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceMaurage, Claude-Alain论文数: 0 引用数: 0 h-index: 0机构: Lille Univ Hosp, Dept Pathol, Lille, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceFigarella-Branger, Dominique论文数: 0 引用数: 0 h-index: 0机构: Marseille Univ Hosp, Dept Pathol, Marseille, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceCoulet, Florence论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, Genet Dept, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceGuerrini-Rousseau, Lea论文数: 0 引用数: 0 h-index: 0机构: Paris Saclay Univ, Dept Pediat & Adolescent Oncol, Gustave Roussy Canc Ctr, Villejuif, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceAlapetite, Claire论文数: 0 引用数: 0 h-index: 0机构: Curie Inst, Dept Radiat Oncol, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceDufour, Christelle论文数: 0 引用数: 0 h-index: 0机构: Paris Saclay Univ, Dept Pediat & Adolescent Oncol, Gustave Roussy Canc Ctr, Villejuif, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceColas, Chrystelle论文数: 0 引用数: 0 h-index: 0机构: Curie Inst, Genet Dept, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceDoz, Francois论文数: 0 引用数: 0 h-index: 0机构: SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, France Paris Descartes Univ, Sorbonne Paris Cite, Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, FranceBourdeaut, Franck论文数: 0 引用数: 0 h-index: 0机构: SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, France SIREDO Canc Ctr Care Innovat & Res Pediat Adolese, Curie Inst, 26 Rue Ulm, F-75005 Paris, France
- [2] LKB1 signaling is activated in CTNNB1-mutated HCC and positively regulates β-catenin-dependent CTNNB1-mutated HCCJOURNAL OF PATHOLOGY, 2019, 247 (04): : 435 - 443Charawi, Sara论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceJust, Pierre-Alexandre论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Hop Univ Paris Ctr, Hop Cochin, AP HP, Dept Pathol, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceSavall, Mathilde论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceAbitbol, Shirley论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceTraore, Massire论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceMetzger, Nolwenn论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceRavinger, Roland论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceCavard, Catherine论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FranceTerris, Benoit论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Hop Univ Paris Ctr, Hop Cochin, AP HP, Dept Pathol, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, FrancePerret, Christine论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France CNRS, Dev Reprod Canc, UMR8104, Paris, France Univ Paris 05, Dev Reprod Canc, Paris, France Equipe Labellisee LNCC, Paris, France Hop Univ Paris Ctr, Hop Cochin, AP HP, Dept Pathol, Paris, France Inst Cochin, Dev Reprod Canc, INSERM, U1016, Paris, France
- [3] LEF1 Immunohistochemistry in the Evaluation of Medulloblastoma SubgroupsJOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2018, 77 (06): : 514 - 515Thomas, Diana论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USA Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USAMurdoch, Geoffrey论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USA Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USAHamilton, Ronald论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USA Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USAOrr, Brent论文数: 0 引用数: 0 h-index: 0机构: St Jude Childrens Res Hosp, 332 N Lauderdale St, Memphis, TN 38105 USA Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USA
- [4] CLINICOPATHOLOGICAL CHARACTERISTICS OF WOMEN WITH CTNNB1-MUTATED ENDOMETRIAL CANCERINTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2021, 31 : A101 - A101Knez, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, Slovenia Univ Maribor, Med Fak, Dept Obstet & Gynecol, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, SloveniaSobocan, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, Slovenia Univ Maribor, Med Fak, Dept Obstet & Gynecol, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, SloveniaKavalar, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Ctr, Dept Pathol, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, SloveniaZupin, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Fak, Ctr Human Mol Genet & Pharmacogen, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, SloveniaBuedefeld, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Fak, Ctr Human Mol Genet & Pharmacogen, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, SloveniaPotocnik, U.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Fak, Ctr Human Mol Genet & Pharmacogen, Maribor, Slovenia Univ Maribor, Fac Chem & Chem Engn, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, SloveniaTakac, I.论文数: 0 引用数: 0 h-index: 0机构: Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, Slovenia Univ Maribor, Med Fak, Dept Obstet & Gynecol, Maribor, Slovenia Univ Maribor, Med Ctr, Div Gyanecol & Perinatol, Maribor, Slovenia
- [5] Expanding the phenotype of CTNNB1-mutated individuals and description of the fetal phenotypeEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 216 - 217Wells, C. F.论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceHeide, S.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, AP HP, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceCharles, P.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Ctr Reference Neurogenet, AP HP, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceMarey, I.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, AP HP, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceHeron, D.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, AP HP, Paris, France Ctr Reference Deficiences Intellectuelles Causes, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceNava, C.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, AP HP, Paris, France Ctr Reference Deficiences Intellectuelles Causes, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceCourtin, T.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, AP HP, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceIsidor, B.论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FrancePiton, A.论文数: 0 引用数: 0 h-index: 0机构: Inst Genet Biol Mol Cellulaire, Dept Translat Med & Neurogenet, Illkirch Graffenstaden, France Hop Univ Strasbourg, Lab Diagnost Genet, Strasbourg, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceGerard, B.论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Lab Diagnost Genet, Strasbourg, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceBuratti, J.论文数: 0 引用数: 0 h-index: 0机构: Inst Pasteur, CNRS, UMR 3571, Genes Synapses & Cognit, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceFradin, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Unite Genet clin, Rennes, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceDubourg, C.论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Unite Genet clin, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FrancePasquier, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Rennes 1, CNRS, UMR6290, Serv Genet,CHU Rennes, Rennes, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceFaivre, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Fac Med, INSERM, LNC,UMR 1231,Equipe GAD, Dijon, France Ctr Hosp Univ Dijon, Ctr Genet, Dijon, France Ctr Hosp Univ Dijon, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FrancePhilip, N.论文数: 0 引用数: 0 h-index: 0机构: APHM, Hop Timone, Dept Med Genet, Marseille, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceMilh, M.论文数: 0 引用数: 0 h-index: 0机构: APHM, Hop Timone, Serv Neurol Pediatr, Marseille, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceLesca, G.论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet, Ctr Reference Anomalies Dev, Bron, France UCB Lyon 1, Ctr Rech Neurosci Lyon, CNRS, INSERM,U1028,UMR5292,GENDEV Team, Lyon, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceEdery, P.论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet, Ctr Reference Anomalies Dev, Bron, France UCB Lyon 1, Ctr Rech Neurosci Lyon, CNRS, INSERM,U1028,UMR5292,GENDEV Team, Lyon, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceSanlaville, D.论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet, Ctr Reference Anomalies Dev, Bron, France UCB Lyon 1, Ctr Rech Neurosci Lyon, CNRS, INSERM,U1028,UMR5292,GENDEV Team, Lyon, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceLiquier, A.论文数: 0 引用数: 0 h-index: 0机构: Lab Cytogenet, Lyon, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceDieux, A.论文数: 0 引用数: 0 h-index: 0机构: Hop Jeanne Flandre, Serv genet clin Guy Fontaine CHRU Lille, Lille, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceAttie-Bitach, T.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Serv Histol Embryol Cytogenet, Paris, France Hop Necker Enfants Malad, Inst Imagine, INSERM, U1163, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceColin, E.论文数: 0 引用数: 0 h-index: 0机构: CHU Angers, Dept Biochim & Genet, Angers, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceBonneau, D.论文数: 0 引用数: 0 h-index: 0机构: CHU Angers, Dept Biochim & Genet, Angers, France CHU Angers, Inst MitoVasc Angers, CNRS, INSERM,UMR6015,U1083,Equipe MitoLab, Angers, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceKeren, B.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, AP HP, Paris, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, FranceGenevieve, D.论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, France CHU Montpellier, Ctr Reference Anomalies Dev & syndrome Malformaif, Maladie Rares & Med Personalisee, Dept Genet Med, Montpellier, France
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