共 50 条
- [21] A novel nonsense variant in ARID1B causing simultaneous RNA decay and exon skipping is associated with Coffin-Siris syndromeHuman Genome Variation, 9Viktoriia Sofronova论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineYu Fukushima论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineMitsuo Masuno论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineMami Naka论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineMiho Nagata论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineYasuki Ishihara论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineYohei Miyashita论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineYoshihiro Asano论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineTakahito Moriwaki论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineRina Iwata论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineSeigo Terawaki论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineYasuko Yamanouchi论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic MedicineTakanobu Otomo论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Medical School,Department of Molecular and Genetic Medicine
- [22] Malignant Rhabdoid Tumour in an Adolescent with Coffin-Siris Syndrome and a Germline ARID1B Mutation: A Case Report and Review of the LiteraturePEDIATRIC BLOOD & CANCER, 2018, 65 : S382 - S382Calley, J.论文数: 0 引用数: 0 h-index: 0机构: Royal Aberdeen Childrens Hosp, Dept Paediat Oncol, Aberdeen, Scotland Royal Aberdeen Childrens Hosp, Dept Paediat Oncol, Aberdeen, ScotlandBrown, P. A. J.论文数: 0 引用数: 0 h-index: 0机构: Aberdeen Royal Infirm, Dept Pathol, Aberdeen, Scotland Royal Aberdeen Childrens Hosp, Dept Paediat Oncol, Aberdeen, ScotlandMorgan, D.论文数: 0 引用数: 0 h-index: 0机构: Royal Aberdeen Childrens Hosp, Dept Radiol, Aberdeen, Scotland Royal Aberdeen Childrens Hosp, Dept Paediat Oncol, Aberdeen, ScotlandBishop, H.论文数: 0 引用数: 0 h-index: 0机构: Royal Aberdeen Childrens Hosp, Dept Paediat Oncol, Aberdeen, Scotland Royal Aberdeen Childrens Hosp, Dept Paediat Oncol, Aberdeen, Scotland
- [23] ARID1B基因突变致Coffin-Siris综合征2例分析中国实用儿科杂志 , 2021, (04) : 299 - 302王俊玲论文数: 0 引用数: 0 h-index: 0机构: 不详方方论文数: 0 引用数: 0 h-index: 0机构: 不详刘志梅论文数: 0 引用数: 0 h-index: 0机构: 不详徐曼婷论文数: 0 引用数: 0 h-index: 0机构: 不详代丽芳论文数: 0 引用数: 0 h-index: 0机构: 不详
- [24] Coffin-Siris综合征携带ARID1B基因变异1例并文献复习甘肃医药, 2022, 41 (10) : 953 - 954+960胡国生论文数: 0 引用数: 0 h-index: 0机构: 阜阳市人民医院李岩论文数: 0 引用数: 0 h-index: 0机构: 阜阳市人民医院张苗苗论文数: 0 引用数: 0 h-index: 0机构: 阜阳市人民医院李亚彬论文数: 0 引用数: 0 h-index: 0机构: 阜阳市人民医院
- [25] Recurrence of ARID1B-related Coffin-Siris Syndrome by possible gonadal mosaicismCLINICAL DYSMORPHOLOGY, 2023, 32 (04) : 180 - 183Uctepe, Eyyup论文数: 0 引用数: 0 h-index: 0机构: Acibadem Ankara Tissue Typing Lab, Ankara, Turkiye Acibadem Ankara Tissue Typing Lab, Ankara, TurkiyeErguner, Bekir论文数: 0 引用数: 0 h-index: 0机构: Sabanci Univ, Dept Mol Biol Genet & Bioengn, Tuzla, Istanbul, Turkiye Acibadem Ankara Tissue Typing Lab, Ankara, TurkiyeSonmez, Fatma Mujgan论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Tech Univ, Fac Med, Dept Child Neurol, Trabzon, Turkiye Private Off, Child Neurol, Trabzon, Turkiye Private Off, Child Neurol, 102 3,Cinnah Cd, TR-06690 Ankara, Turkiye Acibadem Ankara Tissue Typing Lab, Ankara, Turkiye
- [26] Coffin-Siris Syndrome in a Patient with Hirschsprung's Disease-Expanding the Phenotype by Mutation ARID1B: Case Report and Literature ReviewJOURNAL OF PEDIATRIC NEUROLOGY, 2023, 21 (05) : 384 - 387Freitas, Leonardo F.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, Brazil Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, BrazilRibeiro, Lays S.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, Brazil Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, BrazilDuarte, Marcio L.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Sao Paulo, Dept Evidence Based Hlth, Rua Napoleao Barros 865, Sao Paulo, SP, Brazil Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, Brazilda Silva, Mayara O.论文数: 0 引用数: 0 h-index: 0机构: Clin Mega Imagem, Dept Radiol, Santos, SP, Brazil Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, BrazilFerreira, Paula M.论文数: 0 引用数: 0 h-index: 0机构: Clin FORT, Dept Pediat Neurol, Varginha, MG, Brazil Univ Fed Sao Paulo, Dept Radiol, Sao Paulo, SP, Brazil
- [27] The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome (vol 21, pg 1295, 2019)GENETICS IN MEDICINE, 2019, 21 (09) : 2160 - 2161van der Sluijs, Pleuntje J.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsJansen, Sandra论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Dept Human Genet, Nijmegen, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsVergano, Samantha A.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Kings Daughters, Div Med Genet & Metab, Norfolk, VA USA Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsAdachi-Fukuda, Miho论文数: 0 引用数: 0 h-index: 0机构: St Marianna Univ, Sch Med, Dept Pediat, Kawasaki, Kanagawa, Japan Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsAlanay, Yasemin论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Pediat Genet Unit, Dept Pediat, Sch Med, Istanbul, Turkey Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsAlKindy, Adila论文数: 0 引用数: 0 h-index: 0机构: Sultan Qaboos Univ Hosp, Dept Genet, Muscat, Oman Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBaban, Anwar论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, Pediat Cardiol & Cardiac Surg Dept, Rome, Italy IRCCS, Res Inst, Rome, Italy Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBayat, Allan论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp Hvidovre, Copenhagen, Denmark Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBeck-Woedl, Stefanie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Tubingen, Dept Mol Genet & Appl Genom, Tubingen, Germany Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBerry, Katherine论文数: 0 引用数: 0 h-index: 0机构: Shodair Hosp, Dept Med Genet, Helena, MT USA Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBijlsma, Emilia K.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBok, Levinus A.论文数: 0 引用数: 0 h-index: 0机构: Maxima Med Ctr, Dept Pediat, Veldhoven, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsBrouwer, Alwin F. J.论文数: 0 引用数: 0 h-index: 0机构: Nij Smellinghe Hosp, Dept Pediat, Drachten, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlandsvan der Burgt, Ineke论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsCampeau, Philippe M.论文数: 0 引用数: 0 h-index: 0机构: CHU St Justine, Dept Pediat, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, Canada Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsCanham, Natalie论文数: 0 引用数: 0 h-index: 0机构: Northwick Pk Hosp & Clin Res Ctr, North West Thames Reg Genet Serv, Harrow, Middx, England Liverpool Womens Hosp, Cheshire & Merseyside Reg Genet Serv, Crown St, Liverpool, Merseyside, England Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsChrzanowska, Krystyna论文数: 0 引用数: 0 h-index: 0机构: Childrens Mem Hlth Inst, Dept Med Genet, Warsaw, Poland Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsChu, Yoyo W. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Li Ka Shing Fac Med, Dept Pediat & Adolescent Med, Hong Kong, Peoples R China Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsChung, Brain H. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Li Ka Shing Fac Med, Dept Pediat & Adolescent Med, Hong Kong, Peoples R China Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsDahan, Karin论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Ctr Human Genet, Gosselies, Belgium Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsDe Rademaeker, Marjan论文数: 0 引用数: 0 h-index: 0机构: Vrije Univ Brussels, Ctr Med Genet, Brussels, Belgium Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsDestree, Anne论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Ctr Human Genet, Gosselies, Belgium Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsDudding-Byth, Tracy论文数: 0 引用数: 0 h-index: 0机构: Hunter Genet, Newcastle, NSW, Australia Univ Newcastle, GrowUpWell Prior Res Ctr, Newcastle, NSW, Australia Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsEarl, Rachel论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsElcioglu, Nursel论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Pendik Hosp, Dept Pediat Genet, Istanbul, Turkey Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsElias, Ellen R.论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado Denver, Sch Med, Dept Pediat & Genet, Aurora, CO USA Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsFagerberg, Christina论文数: 0 引用数: 0 h-index: 0机构: Odense Univ Hosp, Dept Clin Genet, Odense, Denmark Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsGardham, Alice论文数: 0 引用数: 0 h-index: 0机构: Northwick Pk Hosp & Clin Res Ctr, North West Thames Reg Genet Serv, Harrow, Middx, England Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsGener, Blanca论文数: 0 引用数: 0 h-index: 0机构: Cruces Univ Hosp, Biocruces Hlth Res Inst, Dept Genet, Vizcayam, Spain Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsGerkes, Erica H.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsGrasshoff, Ute论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Tubingen, Dept Mol Genet & Appl Genom, Tubingen, Germany Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlandsvan Haeringen, Arie论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsHeitink, Karin R.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Rehabil Med, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsHerkert, Johanna C.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlandsden Hollander, Nicolette S.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsHorn, Denise论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med Genet & Human Genet, Berlin, Germany Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsHunt, David论文数: 0 引用数: 0 h-index: 0机构: Princess Anne Hosp, Wessex Clin Genet Serv, Southampton, Hants, England Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsKant, Sarina G.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Med, Dept Pediat, Tokyo, Japan Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsKayserili, Hulya论文数: 0 引用数: 0 h-index: 0机构: Koc Univ, Sch Med KUSoM, Dept Med Genet, Istanbul, Turkey Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsKersseboom, Rogier论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Sophia Childrens Hosp, Dept Clin Genet, Rotterdam, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsKilic, Esra论文数: 0 引用数: 0 h-index: 0机构: Hematol Oncol Res & Training Childrens Hosp, Dept Pediat Genet, Ankara, Turkey Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsKrajewska-Walasek, Malgorzata论文数: 0 引用数: 0 h-index: 0机构: Childrens Mem Hlth Inst, Dept Med Genet, Warsaw, Poland Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsLammers, Kylin论文数: 0 引用数: 0 h-index: 0机构: Dayton Childrens Hosp, Dept Med Genet, Dayton, OH USA Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsLaulund, Lone W.论文数: 0 引用数: 0 h-index: 0机构: Odense Univ Hosp, Dept Paediat, Odense, Denmark Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsLederer, Damien论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Ctr Human Genet, Gosselies, Belgium Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsLees, Melissa论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp NHS Fdn Trust, Dept Clin Genet, London, England Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsLopez-Gonzalez, Vanesa论文数: 0 引用数: 0 h-index: 0机构: Hosp Clin Univ Virgen de la Arrixaca, Secc Genet Med, Serv Pediat, IMIB Arrixaca,CIBERERISCIII, Murcia, Spain Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsMaas, Saskia论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Acad Med Ctr, Dept Clin Genet, Amsterdam, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, NetherlandsMancini, Grazia M. S.论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Sophia Childrens Hosp, Dept Clin Genet, Rotterdam, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands
- [28] CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndromeSTEM CELL RESEARCH, 2020, 47Boerstler, Tom论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyWend, Holger论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyKrumbiegel, Mandy论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyKavyanifar, Atria论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Biochem, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyReis, Andre论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyLie, Dieter Chichung论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Biochem, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyWinner, Beate论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, GermanyTuran, Soeren论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Biochem, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Stem Cell Biol, D-91054 Erlangen, Germany
- [29] Coffin–Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B geneEuropean Journal of Human Genetics, 2014, 22 : 1327 - 1329Mari-Anne Vals论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsEve Õiglane-Shlik论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsMargit Nõukas论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsRiina Shor论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsAleksandr Peet论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsMart Kals论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsPaula Ann Kivistik论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsAndres Metspalu论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of PaediatricsKatrin Õunap论文数: 0 引用数: 0 h-index: 0机构: University of Tartu,Department of Paediatrics
- [30] ARID1B基因变异致Coffin-Siris综合征1例报告并文献复习临床儿科杂志, 2021, 39 (04) : 294 - 297+307徐欣论文数: 0 引用数: 0 h-index: 0机构: 南京医科大学附属儿童医院康复科汤健论文数: 0 引用数: 0 h-index: 0机构: 南京医科大学附属儿童医院康复科张丽论文数: 0 引用数: 0 h-index: 0机构: 南京医科大学附属儿童医院康复科陆芬论文数: 0 引用数: 0 h-index: 0机构: 南京医科大学附属儿童医院康复科李红英论文数: 0 引用数: 0 h-index: 0机构: 南京医科大学附属儿童医院康复科