共 50 条
- [31] Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23Pediatric Nephrology, 2009, 24 : 1673 - 1681Alexander Hoischen论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsChristina Landwehr论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsSarah Kabisch论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsXiao-Qi Ding论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsDetlef Trost论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsGerhard Stropahl论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsMarianne Wigger论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsBernhard Radlwimmer论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsRuthild G. Weber论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human GeneticsDieter Haffner论文数: 0 引用数: 0 h-index: 0机构: Rheinische Friedrich-Wilhelms-University,Institute of Human Genetics
- [32] Whole exome sequencing for the diagnosis of genetically unexplained severe or syndromic neurodevelopmental disordersEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 462 - 462论文数: 引用数: h-index:机构:Di Silvestre, Antonio Manuel论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Internal Med & Med Therapeut, Pavia, Italy IRCCS Mondino Fdn, Neurogenet Res Ctr, Pavia, ItalySerpieri, Valentina论文数: 0 引用数: 0 h-index: 0机构: IRCCS Mondino Fdn, Neurogenet Res Ctr, Pavia, Italy Univ Pavia, Dept Mol Med, I-27100 Pavia, Italy IRCCS Mondino Fdn, Neurogenet Res Ctr, Pavia, ItalyDi Biagio, Marta论文数: 0 引用数: 0 h-index: 0机构: IRCCS Mondino Fdn, Neurogenet Res Ctr, Pavia, Italy Univ Pavia, Dept Mol Med, I-27100 Pavia, Italy IRCCS Mondino Fdn, Neurogenet Res Ctr, Pavia, ItalyGana, Simone论文数: 0 引用数: 0 h-index: 0机构: IRCCS Mondino Fdn, Med Genet Unit, Pavia, Italy IRCCS Mondino Fdn, Neurogenet Res Ctr, Pavia, Italy论文数: 引用数: h-index:机构:
- [33] Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGHJOURNAL OF MEDICAL GENETICS, 2006, 43 (04) : 362 - 370Lugtenberg, D论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsde Brouwer, APM论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKleefstra, T论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsOudakker, AR论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsFrints, SGM论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsSchrander-Stumpel, CTRM论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsFryns, JP论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsJensen, LR论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsChelly, J论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsMoraine, C论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsTurner, G论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsVeltman, JA论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsHamel, BCJ论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsde Vries, BBA论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsvan Bokhoven, H论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsYntema, HG论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmengen Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
- [34] Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23PEDIATRIC NEPHROLOGY, 2009, 24 (09) : 1673 - 1681Hoischen, Alexander论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, D-5300 Bonn, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyLandwehr, Christina论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, D-5300 Bonn, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyKabisch, Sarah论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyDing, Xiao-Qi论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Dept Diagnost & Intervent Neuroradiol, D-3000 Hannover, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyTrost, Detlef论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, D-5300 Bonn, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyStropahl, Gerhard论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Rostock, Inst Pathol, Rostock, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyWigger, Marianne论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyRadlwimmer, Bernhard论文数: 0 引用数: 0 h-index: 0机构: German Canc Res Ctr, Div Mol Genet, D-6900 Heidelberg, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyWeber, Ruthild G.论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, D-5300 Bonn, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, GermanyHaffner, Dieter论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, Germany Univ Childrens Hosp, Dept Pediat, D-18057 Rostock, Germany
- [35] High frequency of genomic imbalances detected by array-CGH in patients with syndromic developmental eye anomaliesCHROMOSOME RESEARCH, 2011, 19 : S47 - S48Delahaye, Andree论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, France论文数: 引用数: h-index:机构:Chassaing, Nicolas论文数: 0 引用数: 0 h-index: 0机构: CHU Toulouse, Hop Purpan, Serv Genet Med, Toulouse, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceGerard-Blanluet, Marion论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceBitoun, Pierre论文数: 0 引用数: 0 h-index: 0机构: Hop Jean Verdier Consultat Genet Med, AP HP, Serv Pediat, Bondy, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceToutain, Annick论文数: 0 引用数: 0 h-index: 0机构: CHU Tours, Hop Bretonneau, Dept Genet, Tours, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FrancePassemard, Sandrine论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceLegendre, Marie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, INSERM,U676,Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceVerloes, Alain论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceAboura, Azzedine论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceKaltenbach, Sophie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceDupont, Celine论文数: 0 引用数: 0 h-index: 0机构: Hop Jean Verdier, AP HP, Paris, France Hop Robert Debre, Serv Paris, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceTabet, Anne-Claude论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceAmselem, Serge论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, INSERM,U676,Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FrancePipiras, Eva论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceElion, Jacques论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Hop Robert Debre, AP HP, INSERM,U763,Dept Genet, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceGressens, Pierre论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, INSERM, U676, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, FranceBenzacken, Brigitte论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 13, Hop Jean Verdier, AP HP, Paris, France Univ Paris 13, Hop Robert Debra, INSERM, Serv U676, Paris, France Univ Paris 13, Hop Jean Verdier, AP HP, INSERM,Serv U676, Bondy, France
- [36] Diagnostic array-CGH and exome sequencing in a cohort of patients with neurodevelopmental disorders: genetic heterogeneity and phenotypic variabilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 354 - 355Pelle, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, Italy AOU San Luigi Gonzaga, Dept Med & Oncol, Serv Genet Counseling, Orbassano, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyMandrile, G.论文数: 0 引用数: 0 h-index: 0机构: AOU San Luigi Gonzaga, Dept Med & Oncol, Serv Genet Counseling, Orbassano, TO, Italy AOU San Luigi Gonzaga, Microcitemia, Orbassano, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyDi Gregorio, E.论文数: 0 引用数: 0 h-index: 0机构: AOU Citta Salute & Sci Torino, SC Med Genet, Turin, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyDentelli, P.论文数: 0 引用数: 0 h-index: 0机构: AOU Citta Salute & Sci Torino, SC Med Genet, Turin, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyGiorgio, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Turin, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyPavinato, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Turin, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyTartaglia, M.论文数: 0 引用数: 0 h-index: 0机构: Osped Pediat Bambino Gesu IRCSS, Genet & Rare Dis Res Div, Rome, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyBrusselles, A.论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Dept Oncol & Mol Med, Rome, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyPippucci, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Med & Surg Sci, Bologna, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyDimartino, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Med & Surg Sci, Bologna, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyDe Rubeis, S.论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, New York, NY 10029 USA Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyFerrero, G. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Pediat & Publ Hlth & Pediat Sci, Turin, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyBrusco, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Turin, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, ItalyGiachino, D. F.论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, Italy AOU San Luigi Gonzaga, Dept Med & Oncol, Serv Genet Counseling, Orbassano, TO, Italy Univ Turin, Dept Clin & Biol Sci, Orbassano, TO, Italy
- [37] Retinitis Pigmentosa (Non-syndromic)ATLAS OF INHERITED RETINAL DISEASES, 2018, 1085 : 125 - 130Tsang, Stephen H.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Ophthalmol,Inst Human Nutr, Bernard & Shirlee Brown Glaucoma Lab,Jonas Childr, Columbia Stem Cell Initiat,Vagelos Coll Phys & Su, New York, NY 10027 USA Columbia Univ, Inst Human Nutr, Dept Biomed Engn, Vagelos Coll Phys & Surg, New York, NY 10032 USA Columbia Univ, Inst Human Nutr, Dept Pathol, Vagelos Coll Phys & Surg, New York, NY 10032 USA Columbia Univ, Inst Human Nutr, Dept Cell Biol, Vagelos Coll Phys & Surg, New York, NY 10032 USA Columbia Univ, Dept Ophthalmol, Edward S Harkness Eye Inst, NewYork Presbyterian Hosp, New York, NY 10027 USA Columbia Univ, Dept Ophthalmol,Inst Human Nutr, Bernard & Shirlee Brown Glaucoma Lab,Jonas Childr, Columbia Stem Cell Initiat,Vagelos Coll Phys & Su, New York, NY 10027 USASharma, Tarun论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Ophthalmol, Edward S Harkness Eye Inst, NewYork Presbyterian Hosp, New York, NY 10027 USA Columbia Univ, Dept Ophthalmol,Inst Human Nutr, Bernard & Shirlee Brown Glaucoma Lab,Jonas Childr, Columbia Stem Cell Initiat,Vagelos Coll Phys & Su, New York, NY 10027 USA
- [38] Recurrence Patterns of Odontogenic Keratocysts in Syndromic and Non-Syndromic PatientsJournal of Maxillofacial and Oral Surgery, 2024, 23 : 152 - 158Tim Van Cleemput论文数: 0 引用数: 0 h-index: 0机构: KULeuven,OMFS IMPATH Research Group, Department of Imaging & Pathology, Faculty of MedicineXander Jackers论文数: 0 引用数: 0 h-index: 0机构: KULeuven,OMFS IMPATH Research Group, Department of Imaging & Pathology, Faculty of MedicineMaria Piagkou论文数: 0 引用数: 0 h-index: 0机构: KULeuven,OMFS IMPATH Research Group, Department of Imaging & Pathology, Faculty of MedicineConstantinus Politis论文数: 0 引用数: 0 h-index: 0机构: KULeuven,OMFS IMPATH Research Group, Department of Imaging & Pathology, Faculty of Medicine
- [39] Non-syndromic retinitis pigmentosaPROGRESS IN RETINAL AND EYE RESEARCH, 2018, 66 : 157 - 186Verbakel, Sanne K.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlandsvan Huet, Ramon A. C.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, NetherlandsBoon, Camiel J. F.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Ophthalmol, Leiden, Netherlands Univ Amsterdam, Dept Ophthalmol, Acad Med Ctr, Amsterdam, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlandsden Hollander, Anneke I.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Human Genet, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, NetherlandsCollin, Rob W. J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Human Genet, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, NetherlandsKlaver, Caroline C. W.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Erasmus MC, Dept Ophthalmol, Rotterdam, Netherlands Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, NetherlandsHoyng, Carel B.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, NetherlandsRoepman, Ronald论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Human Genet, Radboud Inst Mol Life Sci, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, NetherlandsKlevering, B. Jeroen论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Ophthalmol, Donders Inst Brain Cognit & Behav, Med Ctr, Nijmegen, Netherlands
- [40] Recurrence Patterns of Odontogenic Keratocysts in Syndromic and Non-Syndromic PatientsJOURNAL OF MAXILLOFACIAL & ORAL SURGERY, 2024, 23 (01): : 152 - 158Van Cleemput, Tim论文数: 0 引用数: 0 h-index: 0机构: KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, Belgium Univ Hosp Leuven, Dept Oral & Maxillofacial Surg, UZLeuven Campus St Rafael,Kapucijnenvoer 33, B-3000 Louvain, Belgium KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, BelgiumJackers, Xander论文数: 0 引用数: 0 h-index: 0机构: KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, Belgium Univ Hosp Leuven, Dept Oral & Maxillofacial Surg, UZLeuven Campus St Rafael,Kapucijnenvoer 33, B-3000 Louvain, Belgium KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, BelgiumPiagkou, Maria论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Fac Hlth Sci, Sch Med, Dept Anat, Athens, Greece KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, BelgiumPolitis, Constantinus论文数: 0 引用数: 0 h-index: 0机构: KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, Belgium Univ Hosp Leuven, Dept Oral & Maxillofacial Surg, UZLeuven Campus St Rafael,Kapucijnenvoer 33, B-3000 Louvain, Belgium KULeuven, Fac Med, Dept Imaging & Pathol, OMFS IMPATH Res Grp, Louvain, Belgium