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- [1] Developmental and Psychiatric Presentations of Inherited Metabolic DisordersPEDIATRIC NEUROLOGY, 2013, 48 (03) : 179 - 187Turnacioglu, Sinan论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Med Ctr, Dept Neurol, Washington, DC 20010 USAGropman, Andrea L.论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Med Ctr, Dept Neurol, Washington, DC 20010 USA Childrens Natl Med Ctr, Dept Neurol, Washington, DC 20010 USA
- [2] Understanding the molecular genetic causes of inherited corneal disordersACTA OPHTHALMOLOGICA, 2015, 93Davidson, A.论文数: 0 引用数: 0 h-index: 0
- [3] Perioperative Recommendations for Corneal Refractive Surgery Patients With Inherited Bleeding DisordersCORNEA, 2024, 43 (12) : 1599 - 1607Moshirfar, Majid论文数: 0 引用数: 0 h-index: 0机构: Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USA Univ Utah, John A Moran Eye Ctr, Sch Med, Salt Lake City, UT USA Utah Lions Eye Bank, Murray, UT USA Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USAReynolds, Jonathon C.论文数: 0 引用数: 0 h-index: 0机构: Noorda Coll Osteopath Med, Provo, UT USA Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USAMoin, Kayvon A.论文数: 0 引用数: 0 h-index: 0机构: Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USA Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USALim, Ming Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Internal Med, Div Hematol & Hematol Malignancies, Salt Lake City, UT USA Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USAStoakes, Isabella M.论文数: 0 引用数: 0 h-index: 0机构: Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USA Kettering Hlth, Dept Ophthalmol, Dayton, OH USA Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USAHoopes, Phillip C.论文数: 0 引用数: 0 h-index: 0机构: Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USA Hoopes Vis Res Ctr, Hoopes Vis, Draper, UT USA
- [4] Rare inherited copy number variants as genetic modifiers of developmental disordersEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 470 - 470Atzori, Marta论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, BelgiumHannes, Laurens论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, BelgiumPelgrims, Elise论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, BelgiumSwillen, Ann论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, BelgiumSifrim, Alejandro论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium KU Leuven Inst Single Cell Omics LISCO, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, BelgiumBreckpot, Jeroen论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, BelgiumAttanasio, Catia论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium
- [5] High-throughtput NGS of 60 Genes Involved in Inherited Corneal DisordersINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)Wang, Xinjing论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USANie, Danyao论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USATurner, Angela论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USAWetherby, Keith论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USAGotez, Kerry论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USAGarafalo, Alexandra论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USAParrish, Rebecca论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USATumminia, Santa J.论文数: 0 引用数: 0 h-index: 0机构: NEI, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USAJohnson, Kory论文数: 0 引用数: 0 h-index: 0机构: NINDS, ITBP, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USAFann, Yang论文数: 0 引用数: 0 h-index: 0机构: NINDS, ITBP, Bethesda, MD 20892 USA NEI, Bethesda, MD 20892 USA
- [6] The diagnostic rate of inherited metabolic disorders by exome sequencing in a cohort of 547 individuals with developmental disordersMOLECULAR GENETICS AND METABOLISM REPORTS, 2021, 29Delanne, Julian论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceHuet, Frederic论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceMoutton, Sebastien论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceNambot, Sophie论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceGrisval, Margot论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceHoucinat, Nada论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceKuentz, Paul论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France CHU Besancon, Biol Mol, Besancon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceSorlin, Arthur论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceCallier, Patrick论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Cytogenet & Genet Mol, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceJean-Marcais, Nolwenn论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceMosca-Boidron, Anne-Laure论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Cytogenet & Genet Mol, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceMau-Them, Frederic Tran论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceDenomme-Pichon, Anne-Sophie论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceVitobello, Antonio论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceLehalle, Daphne论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceEl Chehadeh, Salima论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceFrancannet, Christine论文数: 0 引用数: 0 h-index: 0机构: CHU Clermont Ferrand, Ctr Reference Deficiences Intellectuelles Causes, Serv Genet Med, Clermont Ferrand, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceLebrun, Marine论文数: 0 引用数: 0 h-index: 0机构: CHU St Etienne, Lab Genet, St Etienne, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceLambert, Laetitia论文数: 0 引用数: 0 h-index: 0机构: CHRU Nancy, Serv Genet Clin, Nancy, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceJacquemont, Marie-Line论文数: 0 引用数: 0 h-index: 0机构: CHU La Reunion, Grp Hosp Sud Reunion, Unite Genet Med, Pole Femme Mere Enfant, St Pierre, Reunion, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceGerard-Blanluet, Marion论文数: 0 引用数: 0 h-index: 0机构: Robert Debre Hosp, AP HP, Dept Genet, Paris, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceAlessandri, Jean-Luc论文数: 0 引用数: 0 h-index: 0机构: CHU La Reunion, CH Felix Guyon, Serv Reanimat Neonatale, Pole Femme Mere Enfant, St Denis, Reunion, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceWillems, Marjolaine论文数: 0 引用数: 0 h-index: 0机构: Arnaud Villeneuve Hosp, Reference Ctr Rare Dis Dev Disorders & Multiple C, Dept Med Genet, Montpellier, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceThevenon, Julien论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceChouchane, Mondher论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceDarmency, Veronique论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceFatus-Fauconnier, Clemence论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceGay, Sebastien论文数: 0 引用数: 0 h-index: 0机构: CH William Morey, Serv Pediat, Chalon Sur Saone, Saone & Loire, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceBournez, Marie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceMasurel, Alice论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceLeguy, Vanessa论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceDuffourd, Yannis论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FrancePhilippe, Christophe论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceFeillet, Francois论文数: 0 引用数: 0 h-index: 0机构: Arnaud Villeneuve Hosp, Reference Ctr Rare Dis Dev Disorders & Multiple C, Dept Med Genet, Montpellier, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceFaivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, FranceThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France CHU Dijon Bourgogne, Ctr Reference Malad Rares Deficiences Intellectue, Ctr Genet, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
- [7] INHERITED RECURRENT CORNEAL EROSIONTRANSACTIONS OF THE OPHTHALMOLOGICAL SOCIETIES OF THE UNITED KINGDOM, 1981, 101 (JUL): : 239 - 243BRON, AJ论文数: 0 引用数: 0 h-index: 0BURGESS, SEP论文数: 0 引用数: 0 h-index: 0
- [8] Inherited platelet disordersHAEMOPHILIA, 2012, 18 : 154 - 160Nurden, A. T.论文数: 0 引用数: 0 h-index: 0机构: Hop Xavier Arnozan, CRPP PTIB, F-33604 Pessac, France Hop Xavier Arnozan, CRPP PTIB, F-33604 Pessac, FranceFreson, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Louvain, Ctr Mol & Vasc Biol, Louvain, Belgium Hop Xavier Arnozan, CRPP PTIB, F-33604 Pessac, FranceSeligsohn, U.论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Univ, Sheba Med Ctr, Tel Hashomer & Sackler Fac Med, Amalia Biron Res Inst Thrombosis & Hemostasis, IL-69978 Tel Aviv, Israel Hop Xavier Arnozan, CRPP PTIB, F-33604 Pessac, France
- [9] Inherited disorders of cytokinesCURRENT OPINION IN PEDIATRICS, 2004, 16 (06) : 648 - 658Picard, C论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U550,Fac Med Necker,Unite Immunol & Hematol Pedia, Paris, France Univ Paris 05, Hop Necker Enfants Malad, INSERM, U550,Fac Med Necker,Unite Immunol & Hematol Pedia, Paris, FranceCasanova, JL论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U550,Fac Med Necker,Unite Immunol & Hematol Pedia, Paris, France Univ Paris 05, Hop Necker Enfants Malad, INSERM, U550,Fac Med Necker,Unite Immunol & Hematol Pedia, Paris, France
- [10] Inherited Developmental and Epileptic EncephalopathiesNEUROLOGY INTERNATIONAL, 2021, 13 (04) : 555 - 568Bartolini, Emanuele论文数: 0 引用数: 0 h-index: 0机构: Nuovo Osped Santo Stefano, Neurol Unit, USL Ctr Toscana, I-59100 Prato, Italy Nuovo Osped Santo Stefano, Neurol Unit, USL Ctr Toscana, I-59100 Prato, Italy