共 50 条
- [1] Impact and rates of exonic de novo mutations in patients with intellectual disabilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 226 - 226Pranckeniene, L.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Vilnius, Lithuania Vilnius Univ, Vilnius, Lithuania论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [2] Analysis of parental origin of de novo pathogenic CNVs in patients with intellectual disabilityGENETICS AND MOLECULAR BIOLOGY, 2024, 47 (03)Pereira, Samara Socorro Silva论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Univ Fed Goias, Programa Pos Graduacao Genet & Biol Mol, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, BrazilPinto, Irene Plaza论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, BrazilSantos, Victor Cortazio do Prado论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Univ Fed Goias, Programa Pos Graduacao Genet & Biol Mol, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, BrazilSilva, Rafael Carneiro论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, BrazilCosta, Emilia Oliveira Alves论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazilda Cruz, Alex Silva论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazilda Cruz, Aparecido Divino论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Ctr Estadual Reabilitacao & Readaptacao Dr Henr Sa, Secretaria Estadual Saude Goias, Goiania, GO, Brazil Univ Fed Goias, Programa Pos Graduacao Genet & Biol Mol, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazilda Silva, Claudio Carlos论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Ctr Estadual Reabilitacao & Readaptacao Dr Henr Sa, Secretaria Estadual Saude Goias, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, BrazilMinasi, Lysa Bernardes论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil Pontificia Univ Catol Goias, Escola Ciencias Med & Vida, Programa Pos Graduacao Genet, Nucleo Pesquisa Replicon, Goiania, GO, Brazil
- [3] De Novo Mutations in Moderate or Severe Intellectual DisabilityPLOS GENETICS, 2014, 10 (10):Hamdan, Fadi F.论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaSrour, Myriam论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada Montreal Childrens Hosp, Div Pediat Neurol, Montreal, PQ H3H 1P3, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaCapo-Chichi, Jose-Mario论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaDaoud, Hussein论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaNassif, Christina论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaPatry, Lysanne论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaMassicotte, Christine论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaAmbalavanan, Amirthagowri论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, Canada论文数: 引用数: h-index:机构:Diallo, Ousmane论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaHenrion, Edouard论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaDionne-Laporte, Alexandre论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaFougerat, Anne论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaPshezhetsky, Alexey V.论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaVenkateswaran, Sunita论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Div Neurol, Ottawa, ON K1H 8L1, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaRouleau, Guy A.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, CanadaMichaud, Jacques L.论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Res Ctr, Montreal, PQ, Canada Univ Montreal, Dept Pediat, Montreal, PQ H3C 3J7, Canada Univ Montreal, Dept Neurosci, Montreal, PQ, Canada CHU St Justine, Res Ctr, Montreal, PQ, Canada
- [4] Regulatory de novo mutations underlying intellectual disabilityLIFE SCIENCE ALLIANCE, 2023, 6 (05)Vas, Matias G. De论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandBoulet, Fanny论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandJoshi, Shweta S.论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandGarstang, Myles G.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England Univ Essex, Sch Biol Sci, Colchester, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandKhan, Tahir N.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England Natl Univ Med Sci, Dept Biol Sci, Rawalpindi, Pakistan Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandAtla, Goutham论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England Barcelona Inst Sci & Technol, Ctr Genom Regulat, Regulatory Genom & Diabet, Barcelona, Spain Ctr Invest Biomed Red Diabet & Enfermedades Metab, Barcelona, Spain Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England论文数: 引用数: h-index:机构:Moore, David论文数: 0 引用数: 0 h-index: 0机构: Western Gen Hosp, South East Scotland Reg Genet Serv, Edinburgh, Scotland Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandCebola, Ines论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandZhang, Shuchen论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Inst Reprod & Dev Biol, Fac Med, London, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandCui, Wei论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Inst Reprod & Dev Biol, Fac Med, London, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandLampe, Anne K.论文数: 0 引用数: 0 h-index: 0机构: Western Gen Hosp, South East Scotland Reg Genet Serv, Edinburgh, Scotland Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandLam, Wayne W.论文数: 0 引用数: 0 h-index: 0机构: Western Gen Hosp, South East Scotland Reg Genet Serv, Edinburgh, Scotland Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandFerrer, Jorge论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England Barcelona Inst Sci & Technol, Ctr Genom Regulat, Regulatory Genom & Diabet, Barcelona, Spain Ctr Invest Biomed Red Diabet & Enfermedades Metab, Barcelona, Spain Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandPradeepa, Madapura M.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England Univ Essex, Sch Biol Sci, Colchester, England Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, EnglandAtanur, Santosh S.论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England Imperial Coll London, NIHR Imperial Biomed Res Ctr, ITMAT Data Sci Grp, London, England Univ Edinburgh, Ctr Genom & Expt Med, Edinburgh, Scotland Imperial Coll London, Dept Metab Digest & Reprod, Sect Genet & Genom, London, England
- [5] De novo ARX mutations in female patients with agenesis of the corpus callosum and intellectual disabilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 327 - 328Taveira, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, UF Genet Clin, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceHeide, S.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceMignot, C.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceMilh, M.论文数: 0 引用数: 0 h-index: 0机构: Hop La Timone, APHM, Serv Neuropediat, Marseille, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceRastetter, A.论文数: 0 引用数: 0 h-index: 0机构: UPMC, INSERM, UMR S975, CNRS,UMR 7225,ICM, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceJacquette, A.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceCharles, P.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceMarey, I.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceWhalen, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, UF Genet Clin, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceKeren, B.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, UF Genom Dev, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceNava, C.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Dept Genet, UF Genom Dev, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, FranceHeron, D.论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, APHP, Dept Genet, UF Genet Med,Ctr Reference Deficiences Intellectu, Paris, France Hop Armand Trousseau, APHP, UF Genet Clin, Paris, France
- [6] A novel de novo POGZ mutation in a patient with intellectual disabilityJournal of Human Genetics, 2016, 61 : 357 - 359Bo Tan论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Yongyi Zou论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Yue Zhang论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Rui Zhang论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Jianjun Ou论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Yidong Shen论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Jingping Zhao论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Xiaomei Luo论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Jing Guo论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Lanlan Zeng论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Yiqiao Hu论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Yu Zheng论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Qian Pan论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Desheng Liang论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,Lingqian Wu论文数: 0 引用数: 0 h-index: 0机构: State Key Laboratory of Medical Genetics,
- [7] A novel de novo POGZ mutation in a patient with intellectual disabilityJOURNAL OF HUMAN GENETICS, 2016, 61 (04) : 357 - 359Tan, Bo论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaZou, Yongyi论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaZhang, Yue论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaZhang, Rui论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaOu, Jianjun论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp 2, Inst Mental Hlth, Changsha, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaShen, Yidong论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp 2, Inst Mental Hlth, Changsha, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaZhao, Jingping论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp 2, Inst Mental Hlth, Changsha, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaLuo, Xiaomei论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaGuo, Jing论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaZeng, Lanlan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaHu, Yiqiao论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaZheng, Yu论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaPan, Qian论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaLiang, Desheng论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Hunan Jiahui Genet Hosp, Changsha, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R ChinaWu, Lingqian论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Hunan Jiahui Genet Hosp, Changsha, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China
- [8] ARCHIVIST De novo mutations and severe nonsyndromic intellectual disabilityARCHIVES OF DISEASE IN CHILDHOOD, 2013, 98 (02) : 102 - 102不详论文数: 0 引用数: 0 h-index: 0
- [9] De novo CNVs Identified Using High Resolution SNP Array on Patients with Intellectual DisabilityCYTOGENETIC AND GENOME RESEARCH, 2014, 142 (03)DuPont, B. R.论文数: 0 引用数: 0 h-index: 0机构: Greenwood Genet Ctr, Greenwood, SC 29646 USA Greenwood Genet Ctr, Greenwood, SC 29646 USABruce, K. E.论文数: 0 引用数: 0 h-index: 0机构: Greenwood Genet Ctr, Greenwood, SC 29646 USA Greenwood Genet Ctr, Greenwood, SC 29646 USABartel, F. O.论文数: 0 引用数: 0 h-index: 0机构: Greenwood Genet Ctr, Greenwood, SC 29646 USA Greenwood Genet Ctr, Greenwood, SC 29646 USAChaubey, A.论文数: 0 引用数: 0 h-index: 0机构: Greenwood Genet Ctr, Greenwood, SC 29646 USA Greenwood Genet Ctr, Greenwood, SC 29646 USA
- [10] De novo variants of DEAF1 cause intellectual disability in six Chinese patientsCLINICA CHIMICA ACTA, 2021, 518 : 17 - 21Chen, Shimeng论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaDeng, Xiaolu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaXiong, Juan论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaHe, Fang论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaYang, Lifen论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaChen, Baiyu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaChen, Chen论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaZhang, Ciliu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaYang, Li论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaPeng, Jing论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R ChinaYin, Fei论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Pediat, Xiangya Hosp, Changsha, Peoples R China