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- [31] Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophyJournal of Human Genetics, 2008, 53 : 565 - 572Jorge Oliveira论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularIsabel Soares-Silva论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularIvo Fokkema论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularAna Gonçalves论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularAlexandra Cabral论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularLuísa Diogo论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularLucía Galán论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularAntónio Guimarães论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularIsabel Fineza论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularJohan T. den Dunnen论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética MolecularRosário Santos论文数: 0 引用数: 0 h-index: 0机构: Centro de Genética Médica Dr. Jacinto Magalhães,Unidade de Genética Molecular
- [32] Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantARCHIVES OF NEUROLOGY, 2008, 65 (01) : 137 - 141Clement, Emma M.论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandGodfrey, Caroline论文数: 0 引用数: 0 h-index: 0机构: Guys Hosp, DNA Lab, Genet Ctr, London SE1 9RT, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandTan, Jenny论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Dept Struct Biol & Biochem, Toronto, ON, Canada Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandBrockington, Martin论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandTorelli, Silvia论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandFeng, Lucy论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandBrown, Susan C.论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England论文数: 引用数: h-index:机构:Sewry, Caroline A.论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Robert Jones & Agnes Hunt Orthopaed Hosp, Ctr Inherited Neuromuscular Disorders, Oswestry SY10 7AG, Shrops, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandLongman, Cheryl论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandMein, Rachael论文数: 0 引用数: 0 h-index: 0机构: Guys Hosp, DNA Lab, Genet Ctr, London SE1 9RT, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandAbbs, Steve论文数: 0 引用数: 0 h-index: 0机构: Guys Hosp, DNA Lab, Genet Ctr, London SE1 9RT, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandVajsar, Firi论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Div Neurol, Toronto, ON, Canada Univ Toronto, Hosp Sick Children, Toronto, ON M5G 1X8, Canada Univ Toronto, Fac Med, Toronto, ON, Canada Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandSchachter, Harry论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Dept Struct Biol & Biochem, Toronto, ON, Canada Univ Toronto, Hosp Sick Children, Toronto, ON M5G 1X8, Canada Univ Toronto, Fac Med, Toronto, ON, Canada Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, EnglandMuntoni, Francesco论文数: 0 引用数: 0 h-index: 0机构: Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England Hammersmith Hosp, Univ London Imperial Coll Sci Technol & Med, Dept Paediat, Dubowitz Neuromuscular Unit, London W12 0NN, England
- [33] Maternal Uniparental Isodisomy of Chromosome 6 Reveals a TULP1 Mutation as a Novel Cause of Cone DysfunctionOPHTHALMOLOGY, 2013, 120 (06) : 1239 - 1246Roosing, Susanne论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Inst Genet & Metab Dis, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsvan den Born, L. Ingeborgh论文数: 0 引用数: 0 h-index: 0机构: Rotterdam Eye Hosp, Rotterdam, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsHoyng, Carel B.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Ophthalmol, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsThiadens, Alberta A. H. J.论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Ophthalmol, Rotterdam, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands论文数: 引用数: h-index:机构:Collin, Rob W. J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Inst Genet & Metab Dis, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKoenekoop, Robert K.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Ctr Hlth, McGill Ocular Genet Lab, Montreal, PQ, Canada Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsLeroy, Bart P.论文数: 0 引用数: 0 h-index: 0机构: Univ Ghent, Ctr Med Genet Ghent, B-9000 Ghent, Belgium Ghent Univ Hosp, Dept Ophthalmol, Ghent, Belgium Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsvan Moll-Ramirez, Norka论文数: 0 引用数: 0 h-index: 0机构: Ctr Expertise Blind & Partially Sighted People, Royal Dutch Visio, Grave, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsVenselaar, Hanka论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, CMBI Nijmegen, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsRiemslag, Frans C. C.论文数: 0 引用数: 0 h-index: 0机构: Rotterdam Eye Hosp, Rotterdam, Netherlands Bartimeus Inst Visually Impaired, Zeist, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsCremers, Frans P. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKlaver, Caroline C. W.论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Ophthalmol, Rotterdam, Netherlands Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsden Hollander, Anneke I.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Inst Genet & Metab Dis, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Ophthalmol, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
- [34] Dystroglycanopathy with two novel POMT1 mutations in a Chinese boy with developmental delay and muscular dystrophyEUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2014, 18 (04) : 532 - 535Chong, Yeow Kuan论文数: 0 引用数: 0 h-index: 0机构: Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R ChinaMa, Louis Che Kwan论文数: 0 引用数: 0 h-index: 0机构: United Christian Hosp, Dept Paediat, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R ChinaLo, Kit Lin论文数: 0 引用数: 0 h-index: 0机构: United Christian Hosp, Dept Diagnost Radiol & Organ Imaging, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R ChinaLee, Clary Ka Lai论文数: 0 引用数: 0 h-index: 0机构: United Christian Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R ChinaMak, Chloe Miu论文数: 0 引用数: 0 h-index: 0机构: Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R ChinaKan, Amanda Nim Chi论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R ChinaLam, Ching Wan论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Li Ka Shing Fac Med, Dept Pathol, Hong Kong, Hong Kong, Peoples R China Princess Margaret Hosp, Dept Pathol, Genet Pathol Lab, Hong Kong, Hong Kong, Peoples R China
- [35] Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophyJOURNAL OF HUMAN GENETICS, 2008, 53 (06) : 565 - 572Oliveira, Jorge论文数: 0 引用数: 0 h-index: 0机构: INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalSoares-Silva, Isabel论文数: 0 引用数: 0 h-index: 0机构: INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalFokkema, Ivo论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Ctr Human & Clin Genet, Leiden, Netherlands INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalGoncalves, Ana论文数: 0 引用数: 0 h-index: 0机构: INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalCabral, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat Coimbra, Ctr Desenvolvimento Crianca Luis Borges, Coimbra, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalDiogo, Luisa论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat Coimbra, Serv Metab, Coimbra, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalGalan, Lucia论文数: 0 引用数: 0 h-index: 0机构: Hosp Geral Santo Antonio, Serv Neuropatol, Oporto, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalGuimaraes, Antonio论文数: 0 引用数: 0 h-index: 0机构: Hosp Geral Santo Antonio, Serv Neuropatol, Oporto, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalFineza, Isabel论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat Coimbra, Ctr Desenvolvimento Crianca Luis Borges, Coimbra, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, Portugalden Dunnen, Johan T.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Ctr Human & Clin Genet, Leiden, Netherlands INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, PortugalSantos, Rosario论文数: 0 引用数: 0 h-index: 0机构: INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, Portugal INSA, Ctr Genet Med Dr Jacinto Magalhaes, Unidade Genet Mol, Oporto, Portugal
- [36] POMGnT1 mutations in congenital muscular dystrophy -: Genotype-phenotype correlation and expanded clinical spectrumARCHIVES OF NEUROLOGY, 2006, 63 (10) : 1491 - 1495Biancheri, Roberta论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyBertini, Enrico论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyFalace, Antonio论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyPedemonte, Marina论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyRossi, Andrea论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyD'Amico, Adele论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyScapolan, Sara论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyBergamino, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyPetrini, Stefania论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyCassandrini, Denise论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyBroda, Paolo论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyManfredi, Mario论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyZara, Federico论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalySantorelli, Filippo M.论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyMinetti, Carlo论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, ItalyBruno, Claudio论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci & Rehabil, Muscular & Neurodegenerat Dis Unit, I-16147 Genoa, Italy
- [37] Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis PigmentosaGENES, 2022, 13 (02)Tachibana, Nobutaka论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan论文数: 引用数: h-index:机构:Nomura, Shuhei论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan论文数: 引用数: h-index:机构:Torii, Kaoruko论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanKurata, Kentaro论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanSato, Miho论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanShimakawa, Shuichi论文数: 0 引用数: 0 h-index: 0机构: Osaka Med & Pharmaceut Univ Hosp, Dept Pediat, Takatsuki, Osaka 5698686, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanAzuma, Noriyuki论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Child Hlth & Dev, Dept Ophthalmol & Lab Visual Sci, Tokyo 1578535, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanOgata, Tsutomu论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Biochem, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Med Ctr, Dept Pediat, Hamamatsu, Shizuoka 4328580, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanWada, Yoshinao论文数: 0 引用数: 0 h-index: 0机构: Osaka Womens & Childrens Hosp, Dept Mol Med, Izumi 5941101, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Womens & Childrens Hosp, Dept Mol Med, Izumi 5941101, Japan Osaka Womens & Childrens Hosp, Dept Med Genet, Izumi 5941101, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan论文数: 引用数: h-index:机构:Nishina, Sachiko论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Child Hlth & Dev, Dept Ophthalmol & Lab Visual Sci, Tokyo 1578535, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, JapanHotta, Yoshihiro论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan Hamamatsu Univ Sch Med, Dept Ophthalmol, Hamamatsu, Shizuoka 4313192, Japan
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