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- [41] Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathyNEUROMUSCULAR DISORDERS, 2021, 31Taniguchi-Ikeda, Mariko论文数: 0 引用数: 0 h-index: 0机构: Fujita Hlth Univ Hosp, Toyoake, Aichi, Japan Fujita Hlth Univ Hosp, Toyoake, Aichi, Japan论文数: 引用数: h-index:机构:Chakrabarty, Sanjiban论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Rotterdam, Netherlands Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanKellaris, Georgios论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Durham, NC USA Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanTanboon, Jantima论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Tokyo, Japan Fujita Hlth Univ Hosp, Toyoake, Aichi, Japan论文数: 引用数: h-index:机构:Toda, Tatsushi论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Tokyo, Japan Univ Amsterdam, Amsterdam UMC, Amsterdam, Netherlands Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanGoto, Yu-ichi论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Tokyo, Japan Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanNonaka, Ikuya论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Tokyo, Japan Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanKatsanis, Nicholas论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Durham, NC USA Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanDuijkers, Floor A. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Amsterdam UMC, Amsterdam, Netherlands Fujita Hlth Univ Hosp, Toyoake, Aichi, JapanDe Giorgio, Roberto论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Ferrara, Italy Fujita Hlth Univ Hosp, Toyoake, Aichi, Japan
- [42] Can pathology help in functional interpretation of genetic variants - A case report of Novel variants in NARS2 gene with mitochondrial dysfunction presenting as early infantile epileptic encephalopathy with cardiac and skeletal muscle involvementNEUROLOGY, 2019, 92 (15)Heredia, Wilson论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USALichter-Konecki, Uta论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USAWalsh, Leslie论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USAOzolek, John论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USA UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USAMurdoch, Geoffrey论文数: 0 引用数: 0 h-index: 0机构: UPMC, Presbyterian Hosp, Pathol, Pittsburgh, PA USA UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USARajan, Deepa论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Pittsburgh, Pittsburgh, PA 15213 USA UPMC, Childrens Hosp, Pathol, Pittsburgh, PA USA
- [43] Biallelic truncating variants in VGLL2 cause syngnathia in humansJOURNAL OF MEDICAL GENETICS, 2023, 60 (11) : 1084 - 1091Agostini, Valeria论文数: 0 引用数: 0 h-index: 0机构: Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France Univ Paris Cite, Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceTessier, Aude论文数: 0 引用数: 0 h-index: 0机构: Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France Univ Paris Cite, Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceDjaziri, Nabila论文数: 0 引用数: 0 h-index: 0机构: Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France Univ Paris Cite, Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceKhonsari, Roman Hossein论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Hop Necker Enfants Malad, AP HP, Ctr reference Fentes & Malformat Faciales MAFACE,S, Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceGalliani, Eva论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Hop Necker Enfants Malad, AP HP, Ctr reference Fentes & Malformat Faciales MAFACE,S, Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceKurihara, Yukiko论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Grad Sch Med, Dept Physiol Chem & Metab, Tokyo, Japan Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Hidaka, Kyoko论文数: 0 引用数: 0 h-index: 0机构: Natl Cerebral & Cardiovasc Ctr, Res Inst, Dept Biosci & Genet, Suita, Japan Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceTuncbilek, Gokhan论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Ankara, Turkiye Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France论文数: 引用数: h-index:机构:Konas, Ersoy论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Ankara, Turkiye Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceAmiel, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine, F-75015 Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, FranceGordon, Christopher T.论文数: 0 引用数: 0 h-index: 0机构: Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France Univ Paris Cite, Paris, France Inst Imagine, F-75015 Paris, France Imagine Inst, Lab Embryol & Genet Human Malformat, INSERM, UMR 1163, Paris, France
- [44] Biallelic truncating variants in VGLL2 cause syngnathia in humansEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 75 - 75Gordon, Christopher论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine Embryol & Genet Malformat, Paris, France Inst Imagine Embryol & Genet Malformat, Paris, FranceAgostini, Valeria论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine Embryol & Genet Malformat, Paris, France Inst Imagine Embryol & Genet Malformat, Paris, FranceTessier, Aude论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine Embryol & Genet Malformat, Paris, France Inst Imagine Embryol & Genet Malformat, Paris, FranceKhonsari, Roman论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine Embryol & Genet Malformat, Paris, FranceGalliani, Eva论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Maxillofacial Surg, Paris, France Inst Imagine Embryol & Genet Malformat, Paris, France论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Picard, Arnaud论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Maxillofacial Surg, Paris, France Inst Imagine Embryol & Genet Malformat, Paris, FranceKonas, Ersoy论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Dent, Ankara, Turkiye Inst Imagine Embryol & Genet Malformat, Paris, FranceAmiel, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine Embryol & Genet Malformat, Paris, France Hop Necker Enfants Malad, Serv Med Genom Malad Rares, Paris, France Inst Imagine Embryol & Genet Malformat, Paris, France
- [45] Biallelic variants in DNA2 cause microcephalic primordial dwarfismHUMAN MUTATION, 2019, 40 (08) : 1063 - 1070Tarnauskaite, Zygimante论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandBicknell, Louise S.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandMarsh, Joseph A.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandMurray, Jennie E.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandParry, David A.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandLogan, Clare, V论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandBober, Michael B.论文数: 0 引用数: 0 h-index: 0机构: Alfred I DuPont Hosp Children, Dept Pediat, Div Genet, Wilmington, DE USA Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlanddeSilva, Deepthi C.论文数: 0 引用数: 0 h-index: 0机构: Univ Kelaniya, Fac Med, Dept Physiol, Colombo, Sri Lanka Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandDuker, Angela L.论文数: 0 引用数: 0 h-index: 0机构: Alfred I DuPont Hosp Children, Dept Pediat, Div Genet, Wilmington, DE USA Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandSillence, David论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Discipline Genom Med, Sydney, NSW, Australia Sydney Childrens Hosp Network, Western Sydney Genet Program, Westmead, NSW, Australia Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandWise, Carol论文数: 0 引用数: 0 h-index: 0机构: Rite Hosp Children, Texas Scottish, Sarah M & Charles E Seay Ctr Musculoskeletal Res, Dallas, TX USA Univ Texas Southwestern Med Ctr Dallas, McDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA Univ Texas Southwestern Med Ctr Dallas, Dept Orthopaed Surg, Dallas, TX 75390 USA Univ Texas Southwestern Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandJackson, Andrew P.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Otago, Dunedin Sch Med, Dept Pathol, Dunedin, New Zealand Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandMurina, Olga论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, ScotlandReijns, Martin A. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland
- [46] Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorderGENETICS IN MEDICINE, 2024, 26 (05)Accogli, Andrea论文数: 0 引用数: 0 h-index: 0机构: McGill Univ Hlth Ctr MUHC, Dept Specialized Med, Div Med Genet, Montreal, PQ, Canada McGill Univ, Dept Human Genet, Montreal, PQ, Canada Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAPark, Young N.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USA Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USALenk, Guy M.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USA Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USASeverino, Mariasavina论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Neuroradiol Unit, Genoa, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAScala, Marcello论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Ist Giannina Gaslini, Pediat Neurol & Muscular Dis Unit, Genoa, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USADenecke, Jonas论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Univ Childrens Hosp, Hamburg, Germany Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAHempel, Maja论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USALessel, Davor论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAKortuem, Fanny论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USASalpietro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: UCL, Queen Sq Inst Neurol, Dept Neuromuscular Disorders, London, England Univ Aquila, Dept Biotechnol & Appl Clin Sci, I-67100 Laquila, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAde Marco, Patrizia论文数: 0 引用数: 0 h-index: 0机构: IRCCS G Gaslini, UOC Genet Med, Genoa, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAGuerrisi, Sara论文数: 0 引用数: 0 h-index: 0机构: IRCCS G Gaslini, UOC Genet Med, Genoa, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USATorella, Annalaura论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med TIGEM, Naples, Italy Univ Campania Luigi Vanvitelli, Dept Precis Med, Naples, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USANigro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med TIGEM, Naples, Italy Univ Campania Luigi Vanvitelli, Dept Precis Med, Naples, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USASrour, Myriam论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ, Canada McGill Univ, Dept Pediat, Div Pediat Neurol, Montreal, PQ, Canada McGill Univ Hlth Ctr MUHC, Res Inst, Montreal, PQ, Canada McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USATurro, Ernest论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY USA Icahn Sch Med Mt Sinai, Mindich Child Hlth & Dev Inst, New York, NY USA Icahn Sch Med Mt Sinai, Charles Bronfman Inst Personalized Med, New York, NY USA Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USALabarque, Veerle论文数: 0 引用数: 0 h-index: 0机构: Univ Leuven, Ctr Mol & Vasc Biol, Dept Cardiovasc Sci, Leuven, Belgium Univ Hosp Leuven, Paediat Hematooncol, Leuven, Belgium Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAFreson, Kathleen论文数: 0 引用数: 0 h-index: 0机构: Univ Leuven, Ctr Mol & Vasc Biol, Dept Cardiovasc Sci, Leuven, Belgium Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAPiatelli, Gianluca论文数: 0 引用数: 0 h-index: 0机构: Gaslini Children s Hosp, Dept Neurosurg, Genoa, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USACapra, Valeria论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist G Gaslini, Genom & Clin Genet, Genoa, Italy Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAKitzman, Jacob O.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USA Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USAMeisler, Miriam H.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USA Univ Michigan, Dept Human Genet, 4808 Med Sci 2, Ann Arbor, MI USA
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- [49] Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomaliesEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (05) : 611 - 618Reuter, Miriam S.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, CGEn, Toronto, ON, Canada Hosp Sick Children, Ctr Appl Genom, Toronto, ON, Canada Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada Hosp Sick Children, CGEn, Toronto, ON, CanadaZech, Michael论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany Tech Univ Munich, Sch Med, Inst Human Genet, Klinikum Rechts Isar, Munich, Germany Hosp Sick Children, CGEn, Toronto, ON, CanadaHempel, Maja论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Hosp Sick Children, CGEn, Toronto, ON, CanadaAltmueller, Janine论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Hosp Cologne, Cologne, Germany Hosp Sick Children, CGEn, Toronto, ON, CanadaHeung, Tracy论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON, Canada Hosp Sick Children, CGEn, Toronto, ON, CanadaPoelsler, Laura论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Inst Human Genet, Innsbruck, Austria Hosp Sick Children, CGEn, Toronto, ON, CanadaSanter, Rene论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, Germany Hosp Sick Children, CGEn, Toronto, ON, Canada论文数: 引用数: h-index:机构:Trost, Brett论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Ctr Appl Genom, Toronto, ON, Canada Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada Hosp Sick Children, CGEn, Toronto, ON, CanadaKubisch, Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Hosp Sick Children, CGEn, Toronto, ON, CanadaScherer, Stephen W.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Ctr Appl Genom, Toronto, ON, Canada Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada Univ Toronto, Dept Mol Genet, Toronto, ON, Canada Univ Toronto, McLaughlin Ctr, Toronto, ON, Canada Hosp Sick Children, CGEn, Toronto, ON, CanadaRudnik-Schoneborn, Sabine论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Inst Human Genet, Innsbruck, Austria Hosp Sick Children, CGEn, Toronto, ON, CanadaBassett, Anne S.论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON, Canada Univ Hlth Network, Toronto Congenital Cardiac Ctr Adults, Peter Munk Cardiac Ctr, Div Cardiol,Dept Med, Toronto, ON, Canada Univ Hlth Network, Dalglish Family 22q Clin Adults 22Q11 2 Delet Syn, Dept Psychiat, Toronto, ON, Canada Univ Hlth Network, Toronto Gen Hosp Res Inst, Toronto, ON, Canada Univ Toronto, Dept Psychiat, Toronto, ON, Canada Hosp Sick Children, CGEn, Toronto, ON, CanadaLessel, Davor论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Hosp Sick Children, CGEn, Toronto, ON, Canada
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