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- [1] miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disabilityBMC GENOMICS, 2013, 14Qiao, Ying论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada Univ British Columbia, Dept Med Genet, BC Child & Family Res Inst, Vancouver, BC V6H 3N1, Canada Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, CanadaBadduke, Chansonette论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, CanadaMercier, Eloi论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Ctr High Biol, Michael Smith Labs 177, Vancouver, BC V6T 1Z4, Canada Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, CanadaLewis, Suzanne M. E.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Med Genet, BC Child & Family Res Inst, Vancouver, BC V6H 3N1, Canada Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, CanadaPavlidis, Paul论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Ctr High Biol, Michael Smith Labs 177, Vancouver, BC V6T 1Z4, Canada Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, CanadaRajcan-Separovic, Evica论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada Univ British Columbia, Dept Pathol & Lab Med, BC Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada
- [2] Copy number variations in Saudi family with intellectual disability and epilepsyBMC GENOMICS, 2015, 17Naseer, Muhammad I.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaChaudhary, Adeel G.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaRasool, Mahmood论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaKalamegam, Gauthaman论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAshgan, Fai T.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAssidi, Mourad论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAhmed, Farid论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAnsari, Shakeel A.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaZaidi, Syed Kashif论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaJan, Mohammed M.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Fac Med, Dept Pediat, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAl-Qahtani, Mohammad H.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia
- [3] Copy Number Variations in aTurkish Cohort of Children with Intellectual DisabilityEXPERIMED, 2023, 13 (03): : 263 - 275Sunnetci-Akkoyunlu, Deniz论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeKara, Bulent论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Child Hlth & Dis, Pediat Neurol, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeCine, Naci论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeEren-Keskin, Seda论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeDogruoglu, Buket论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeIlkay, Zeynep论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeOzer, Tolgahan论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, TurkiyeSavli, Hakan论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye Kocaeli Univ, Fac Med, Dept Med Genet, Kocaeli, Turkiye
- [4] Copy number variations in Saudi family with intellectual disability and epilepsyBMC Genomics, 17Muhammad I. Naseer论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchAdeel G. Chaudhary论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMahmood Rasool论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchGauthaman Kalamegam论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchFai T. Ashgan论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMourad Assidi论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchFarid Ahmed论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchShakeel A. Ansari论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchSyed Kashif Zaidi论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMohammed M. Jan论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMohammad H. Al-Qahtani论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine Research
- [5] Phenotype profiling of patients with intellectual disability and copy number variationsEUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2014, 18 (05) : 558 - 566Rosello, Monica论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, SpainMartinez, Francisco论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, SpainMonfort, Sandra论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, SpainMayo, Sonia论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, SpainOltra, Silvestre论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, SpainOrellana, Carmen论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain Hosp Univ & Politecn La Fe, Unidad Genet & Diagnost Prenatal, Valencia 46009, Spain
- [6] COPY NUMBER VARIATIONS IN ADULTS WITH INTELLECTUAL DISABILITY AND NEUROPSYCHIATRIC DISORDERSJOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2014, 58 (10) : 888 - 888Strydom, A.论文数: 0 引用数: 0 h-index: 0机构: UCL, Div Psychiat, London, England UCL, Div Psychiat, London, EnglandWolfe, K.论文数: 0 引用数: 0 h-index: 0机构: UCL, Div Psychiat, London, England UCL, Div Psychiat, London, EnglandMcquillin, A.论文数: 0 引用数: 0 h-index: 0机构: UCL, Div Psychiat, London, England UCL, Div Psychiat, London, EnglandBass, N.论文数: 0 引用数: 0 h-index: 0机构: UCL, Div Psychiat, London, England UCL, Div Psychiat, London, England
- [7] Copy Number Variations Burden on miRNA Genes Reveals Layers of Complexities Involved in the Regulation of Pathways and Phenotypic ExpressionPLOS ONE, 2014, 9 (02):Veerappa, Avinash M.论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaMurthy, Megha N.论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaVishweswaraiah, Sangeetha论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaLingaiah, Kusuma论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaSuresh, Raviraj V.论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaNachappa, Somanna Ajjamada论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaPrashali, Nelchi论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaYadav, Sangeetha Nuggehalli论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaSrikanta, Manjula Arsikere论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaManjegowda, Dinesh S.论文数: 0 引用数: 0 h-index: 0机构: Yenepoya Univ, Yenepoya Med Coll, Dept Anat, Mangalore, Karnataka, India Nitte Univ, KS Hegde Med Acad, Ctr Sci Educ & Res, Mangalore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaSeshachalam, Keshava B.论文数: 0 引用数: 0 h-index: 0机构: JSS Hosp, Dept Neurol, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, IndiaRamachandra, Nallur B.论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India Univ Mysore, Dept Studies Zool, Genet & Genom Lab, Mysore, Karnataka, India
- [8] Rare Copy Number Variations and Predictors in Children With Intellectual Disability and EpilepsyFRONTIERS IN NEUROLOGY, 2018, 9论文数: 引用数: h-index:机构:Xiong, Juan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaWu, Liwen论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaYang, Lifen论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaHe, Fang论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China论文数: 引用数: h-index:机构:Pang, Nan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaDuan, Haolin论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaZhang, Wen论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaArafat, Ahmed论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaYin, Fei论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaPeng, Jing论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China
- [9] Acquired copy number alterations of miRNA genes in acute myeloid leukemia are uncommonBLOOD, 2013, 122 (15) : E44 - E51Ramsingh, Giridharan论文数: 0 引用数: 0 h-index: 0机构: Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USAJacoby, Meagan A.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USAShao, Jin论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USAPizzaro, Rigoberto E. De Jesus论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USAShen, Dong论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca, Gaithersburg, MD USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USATrissal, Maria论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USAGetz, Angela H.论文数: 0 引用数: 0 h-index: 0机构: Univ So Mississippi, Dept Biol Sci, Hattiesburg, MS 39406 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USALey, Timothy J.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USAWalter, Matthew J.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USALink, Daniel C.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Div Oncol, Sch Med, Dept Med, St Louis, MO 63110 USA Univ So Calif, Dept Med, Jane Anne Nohl Div Hematol, Los Angeles, CA USA
- [10] Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual DisabilityJOURNAL OF PEDIATRICS, 2017, 185 : 160 - +Heide, Solveig论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France UPMC, GRC Intellectual Disabil & Autism, Paris, France UPMC, Sorbonne Univ, CNRS UMR 7225, Univ Paris 06,UMR S 1127,Inserm U1127,ICM, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceKeren, Boris论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Genet, Unit Dev Genom, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, Francede Villemeur, Thierry Billette论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, AP HP, Div Pediat Neurol, Paris, France UPMC, GRC ConCer LD, Paris, France INSERM, U1141, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceChantot-Bastaraud, Sandra论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, AP HP, Dept Genet, Div Chromosomal Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceDepienne, Christel论文数: 0 引用数: 0 h-index: 0机构: UPMC, Sorbonne Univ, CNRS UMR 7225, Univ Paris 06,UMR S 1127,Inserm U1127,ICM, Paris, France GH Pitie Salpetriere, AP HP, Dept Genet, Unit Dev Genom, Paris, France Univ Strasbourg, CNRS UMR 7104, INSERM U964, IGBMC,Dept Translat Med & Neurogenet, Illkirch Graffenstaden, France Hop Univ Strasbourg, Inst Med Genet Alsace, Div Cytogenet, Strasbourg, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France论文数: 引用数: h-index:机构:Mignot, Cyril论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceJacquette, Aurelia论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceFonteneau, Eric论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Genet, Unit Dev Genom, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceLejeune, Elodie论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Genet, Unit Dev Genom, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceMach, Corinne论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Genet, Unit Dev Genom, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceMarey, Isabelle论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceWhalen, Sandra论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, AP HP, Dept Genet, Div Clin Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France论文数: 引用数: h-index:机构:Naudion, Sophie论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, CHU Bordeaux, INSERM, U1211,Div Med Genet, Bordeaux, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceRooryck, Caroline论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, CHU Bordeaux, INSERM, U1211,Div Med Genet, Bordeaux, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceToutain, Annick论文数: 0 引用数: 0 h-index: 0机构: CHU Tours, Hop Bretonneau, Div Genet, Tours, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceLe Caignec, Cedric论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, CNRS ERL3147, Inserm UMR 915, Inst Biol,Div Med Genet, Nantes, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceHaye, Damien论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Div Med Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceOlivier-Faivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Hop Enfants, Genet Ctr, FHU TRANSLAD, Dijon, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceMasurel-Paulet, Alice论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Hop Enfants, Genet Ctr, FHU TRANSLAD, Dijon, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Hop Enfants, Genet Ctr, FHU TRANSLAD, Dijon, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceLesne, Fabien论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceFaudet, Anne论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceVille, Dorothee论文数: 0 引用数: 0 h-index: 0机构: GH Est, HCL, Div Pediat Neurol, Bron, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, Francedes Portes, Vincent论文数: 0 引用数: 0 h-index: 0机构: GH Est, HCL, Div Pediat Neurol, Bron, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceSanlaville, Damien论文数: 0 引用数: 0 h-index: 0机构: HCL, Div Genet, Bron, France Univ Claude BernardLyon 1, UMR CNRS 5292, Ctr Res Neurosci Lyon, Inserm U1028,GENDEV Team, Lyon, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceSiffroi, Jean-Pierre论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, AP HP, Dept Genet, Div Chromosomal Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceMoutard, Marie-Laure论文数: 0 引用数: 0 h-index: 0机构: UPMC, GRC ConCer LD, Paris, France INSERM, U1141, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, FranceHeron, Delphine论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France UPMC, GRC Intellectual Disabil & Autism, Paris, France UPMC, Sorbonne Univ, CNRS UMR 7225, Univ Paris 06,UMR S 1127,Inserm U1127,ICM, Paris, France Hop Armand Trousseau, AP HP, Dept Genet, Div Clin Genet, Paris, France GH Pitie Salpetriere, AP HP, Ref Ctr Intellectual Disabil Rare Causes, Dept Genet,Unit Med Genet, Paris, France