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- [1] Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivityBRAIN, 2019, 142 : 3963 - 3974Gregory, Michael D.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USAMervis, Carolyn B.论文数: 0 引用数: 0 h-index: 0机构: Univ Louisville, Neurodev Sci Lab, Dept Psychol & Brain Sci, Louisville, KY 40292 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USAElliott, Maxwell L.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USAKippenhan, J. Shane论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USANash, Tiffany论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USACzarapata, Jasmin B.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USAPrabhakaran, Ranjani论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USARoe, Katherine论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USAEisenberg, Daniel P.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USAKohn, Philip D.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USABerman, Karen F.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Psychosis & Cognit Studies Sect, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Clin & Translat Neurosci Branch, Intramural Res Program,NIH, Bethesda, MD 20892 USA
- [2] Genetic Variation in the Williams Syndrome Gene LIMK1 Affects Resting Functional Connectivity Between Dorsal and Ventral Visual Processing StreamsBIOLOGICAL PSYCHIATRY, 2013, 73 (09) : 147S - 147SGregory, Michael D.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USAKippenhan, J. Shane论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USAXiao, Ena论文数: 0 引用数: 0 h-index: 0机构: NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USATong, Yunxia论文数: 0 引用数: 0 h-index: 0机构: NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USAKolachana, Bhaskar S.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USAWeinberger, Daniel R.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USAMattay, Venkata S.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USABerman, Karen F.论文数: 0 引用数: 0 h-index: 0机构: NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA NIMH, Sect Integrat Neuroimaging, Intramural Res Program, Bethesda, MD 20892 USA
- [3] In-depth analysis of spatial cognition in Williams syndrome:: A critical assessment of the role of the LIMK1 geneNEUROPSYCHOLOGIA, 2006, 44 (05) : 679 - 685Gray, V论文数: 0 引用数: 0 h-index: 0机构: RLCH Alder Hey, Psychol Serv, Liverpool L12 2AP, Merseyside, EnglandKarmiloff-Smith, A论文数: 0 引用数: 0 h-index: 0机构: RLCH Alder Hey, Psychol Serv, Liverpool L12 2AP, Merseyside, EnglandFunnell, E论文数: 0 引用数: 0 h-index: 0机构: RLCH Alder Hey, Psychol Serv, Liverpool L12 2AP, Merseyside, EnglandTassabehji, M论文数: 0 引用数: 0 h-index: 0机构: RLCH Alder Hey, Psychol Serv, Liverpool L12 2AP, Merseyside, England
- [4] SEQUENCE AND COPY NUMBER ANALYSES OF HEXB GENE IN PATIENTS AFFECTED BY SANDHOFF DISEASE: FUNCTIONAL CHARACTERIZATION OF 9 NOVEL SEQUENCE VARIANTSJOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 : S104 - S104Zampieri, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Maria Misericordia, Udine, Italy Univ Hosp S Maria Misericordia, Udine, ItalyCattarossi, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Maria Misericordia, Udine, Italy Univ Hosp S Maria Misericordia, Udine, ItalyOller Ramirez, A. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Cordoba, Cordoba, Argentina Univ Hosp S Maria Misericordia, Udine, ItalyRosano, C.论文数: 0 引用数: 0 h-index: 0机构: IRCSS San Martino, Genoa, Italy Univ Hosp S Maria Misericordia, Udine, ItalyLourenco, C. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Sao Paulo, Brazil Univ Hosp S Maria Misericordia, Udine, ItalyPasson, N.论文数: 0 引用数: 0 h-index: 0机构: Univ Udine, I-33100 Udine, Italy Univ Hosp S Maria Misericordia, Udine, ItalyMoroni, I论文数: 0 引用数: 0 h-index: 0机构: Fdn Ist Neurol Besta, Milan, Italy Univ Hosp S Maria Misericordia, Udine, ItalyUziel, G.论文数: 0 引用数: 0 h-index: 0机构: Fdn Ist Neurol Besta, Milan, Italy Univ Hosp S Maria Misericordia, Udine, ItalyPettinari, A.论文数: 0 引用数: 0 h-index: 0机构: Osped Riuniti Ancona, Ancona, Italy Univ Hosp S Maria Misericordia, Udine, ItalyStanzial, F.论文数: 0 引用数: 0 h-index: 0机构: Azienda Sanit Alto Adige, Bolzano, Italy Univ Hosp S Maria Misericordia, Udine, ItalyDodelson de Kremer, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Cordoba, Cordoba, Argentina Univ Hosp S Maria Misericordia, Udine, ItalyAzar, N. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Cordoba, Cordoba, Argentina Univ Hosp S Maria Misericordia, Udine, ItalyFilocamo, M.论文数: 0 引用数: 0 h-index: 0机构: IRCCS G Gaslini, Genoa, Italy Univ Hosp S Maria Misericordia, Udine, ItalyBembi, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Maria Misericordia, Udine, Italy Univ Hosp S Maria Misericordia, Udine, ItalyDardis, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Maria Misericordia, Udine, Italy Univ Hosp S Maria Misericordia, Udine, Italy
- [5] Sequence and Copy Number Analyses of HEXB Gene in Patients Affected by Sandhoff Disease: Functional Characterization of 9 Novel Sequence VariantsPLOS ONE, 2012, 7 (07):Zampieri, Stefania论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyCattarossi, Silvia论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyOller Ramirez, Ana Maria论文数: 0 引用数: 0 h-index: 0机构: Univ Cordoba, CEMECO, Ctr Estudio Metabolopatias Congenitas, Cordoba, Argentina Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyRosano, Camillo论文数: 0 引用数: 0 h-index: 0机构: Ist Nazl Ric Canc, Patol Mol Integrata AOU IRCSS San Martino IST, I-16132 Genoa, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyLourenco, Charles Marques论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Clin Hosp Ribeirao Preto, Med Genet Serv, Sao Paulo, Brazil Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyPasson, Nadia论文数: 0 引用数: 0 h-index: 0机构: Univ Udine, Dipartimento Sci Med & Biol, I-33100 Udine, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyMoroni, Isabella论文数: 0 引用数: 0 h-index: 0机构: Fdn Ist Neurol Besta, Dept Child Neurol, Milan, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyUziel, Graziella论文数: 0 引用数: 0 h-index: 0机构: Fdn Ist Neurol Besta, Dept Child Neurol, Milan, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyPettinari, Antonella论文数: 0 引用数: 0 h-index: 0机构: Osped Riuniti Ancona, Clin Pediat, Med Genet Lab, Ancona, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyStanzial, Franco论文数: 0 引用数: 0 h-index: 0机构: Azienda Sanit Alto Adige, Ctr Prov Coordinamento Rete Malattie Rare, Serv Consulenza Genet, Bolzano, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyDodelson de Kremer, Raquel论文数: 0 引用数: 0 h-index: 0机构: Univ Cordoba, CEMECO, Ctr Estudio Metabolopatias Congenitas, Cordoba, Argentina Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyBeatriz Azar, Nydia论文数: 0 引用数: 0 h-index: 0机构: Univ Cordoba, CEMECO, Ctr Estudio Metabolopatias Congenitas, Cordoba, Argentina Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyHazan, Filiz论文数: 0 引用数: 0 h-index: 0机构: Fac Med, Dept Genet, Izmir, Turkey Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyFilocamo, Mirella论文数: 0 引用数: 0 h-index: 0机构: Ist Giannina Gaslini, Lab Diagnosi Prepostnatale Malattie Met, UOSD, Genoa, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyBembi, Bruno论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, ItalyDardis, Andrea论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, Italy Univ Hosp Santa Maria della Misericordia, Reg Coordinator Ctr Rare Dis, Udine, Italy
- [6] Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosomeHUMAN MOLECULAR GENETICS, 2019, 28 (16) : 2785 - 2798Shi, Wentao论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Tianjin Med Univ, Sch Basic Med Sci, Dept Genet, Tianjin 300070, Peoples R China Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandLouzada, Sandra论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandGrigorova, Marina论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Inst Biomed & Translat Med, EE-50411 Tartu, Estonia Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandMassaia, Andrea论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Imperial Coll London, Natl Heart & Lung Inst, London SW7 2AZ, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandArciero, Elena论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandKibena, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Inst Biomed & Translat Med, EE-50411 Tartu, Estonia Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandGe, Xiangyu Jack论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Univ Manchester, Fac Biol Med & Hlth, Sch Biol Sci, Div Musculoskeletal & Dermatol Sci, Manchester M13 9PL, Lancs, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandChen, Yuan论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandAyub, Qasim论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Monash Univ Malaysia, Trop Med & Biol Multidisciplinary Platform, Genom Facil, Bandar Sunway, Selangor Darul Ehsan 47500, Malaysia Monash Univ Malaysia, Sch Sci, Bandar Sunway, Selangor Darul Ehsan 47500, Malaysia Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandPoolamets, Olev论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, Androl Unit, EE-50406 Tartu, Estonia Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandTyler-Smith, Chris论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England论文数: 引用数: h-index:机构:Laan, Maris论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Inst Biomed & Translat Med, EE-50411 Tartu, Estonia Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, EnglandYang, Fengtang论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England论文数: 引用数: h-index:机构:Xue, Yali论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England
- [7] SCREENING SLC2A1 GENE FOR SEQUENCE AND COPY NUMBER VARIATIONS ASSOCIATED WITH GLUT-1 DEFICIENCY SYNDROMEJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, 2020, 83 (03): : 177 - 183Ornek Erguzeloglu, Cemre论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey Uludag Univ, Dept Med Genet, Fac Med, Bursa, Turkey Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyKara, Bulent论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Dept Pediat Neurol, Fac Med, Kocaeli, Turkey Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyKaracan, Ilker论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey Istanbul Medeniyet Univ, Fac Engn & Nat Sci, Dept Mol Biol & Genet, Istanbul, Turkey Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyOzdemir, Ozkan论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey Univ Cologne, Univ Hosp Cologne, Ctr Mol Med Cologne CMMC, Cologne, Germany Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyKesim, Yesim论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey Oxford Brookes Univ, Fac Hlth & Life Sci, Oxford, England Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyBebek, Nerses论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyOzbek, Ugur论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey Mehmet Ali Aydinlar Acibadem Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, TurkeyUgur Iseri, Sibel Aylin论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Genet, Istanbul, Turkey
- [8] Hereditary variation in platelet integrin alpha(2)beta(1) copy number is associated with two silent polymorphisms in the alpha(2) gene sequence.MOLECULAR BIOLOGY OF THE CELL, 1996, 7 : 2481 - 2481Kunicki, TJ论文数: 0 引用数: 0 h-index: 0机构: Scripps Res Inst, DEPT MOL & EXPT MED, LA JOLLA, CA 92037 USAKRitzik, MR论文数: 0 引用数: 0 h-index: 0机构: Scripps Res Inst, DEPT MOL & EXPT MED, LA JOLLA, CA 92037 USAAnnis, DS论文数: 0 引用数: 0 h-index: 0机构: Scripps Res Inst, DEPT MOL & EXPT MED, LA JOLLA, CA 92037 USANugent, DJ论文数: 0 引用数: 0 h-index: 0机构: Scripps Res Inst, DEPT MOL & EXPT MED, LA JOLLA, CA 92037 USA
- [9] EVOLUTION OF NUCLEAR GENE FAMILIES IN PRIMATES - COPY-NUMBER VARIATION IN THE ARGININOSUCCINATE SYNTHETASE (ASS) PSEUDOGENE FAMILY AND THE ANONYMOUS DNA-SEQUENCE, D1S1GENETICA, 1987, 73 (1-2) : 91 - 98DAIGER, SP论文数: 0 引用数: 0 h-index: 0机构: UNIV TEXAS,HLTH SCI CTR,DEPT CELLULAR & STRUCT BIOL,SAN ANTONIO,TX 78284 UNIV TEXAS,HLTH SCI CTR,DEPT CELLULAR & STRUCT BIOL,SAN ANTONIO,TX 78284GOODE, ME论文数: 0 引用数: 0 h-index: 0机构: UNIV TEXAS,HLTH SCI CTR,DEPT CELLULAR & STRUCT BIOL,SAN ANTONIO,TX 78284 UNIV TEXAS,HLTH SCI CTR,DEPT CELLULAR & STRUCT BIOL,SAN ANTONIO,TX 78284TROWBRIDGE, BD论文数: 0 引用数: 0 h-index: 0机构: UNIV TEXAS,HLTH SCI CTR,DEPT CELLULAR & STRUCT BIOL,SAN ANTONIO,TX 78284 UNIV TEXAS,HLTH SCI CTR,DEPT CELLULAR & STRUCT BIOL,SAN ANTONIO,TX 78284
- [10] Diagnosing Smith-Magenis syndrome and duplication 17p11.2 syndrome by RAI1 gene copy number variation using quantitative real-time PCRGENETIC TESTING, 2008, 12 (01): : 67 - 73Truong, Hoa T.论文数: 0 引用数: 0 h-index: 0机构: Charles Sturt Univ, Fac Sci, Wagga Wagga, NSW, Australia Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USASolaymani-Kohal, Sara论文数: 0 引用数: 0 h-index: 0机构: Univ W England, Bristol BS16 1QY, Avon, England Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USABaker, Kevin R.论文数: 0 引用数: 0 h-index: 0机构: Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury, Wilts, England Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USAGirirajan, Santhosh论文数: 0 引用数: 0 h-index: 0机构: Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USA Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USAWilliams, Stephen R.论文数: 0 引用数: 0 h-index: 0机构: Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USA Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USAVlangos, Christopher N.论文数: 0 引用数: 0 h-index: 0机构: Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USA Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USASmith, Ann C. M.论文数: 0 引用数: 0 h-index: 0机构: NHGRI, NIH, Bethesda, MD 20892 USA Georgetown Univ, Med Ctr, Washington, DC 20007 USA Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USABunyan, David J.论文数: 0 引用数: 0 h-index: 0机构: Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury, Wilts, England Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USARoffey, Paul E.论文数: 0 引用数: 0 h-index: 0机构: Charles Sturt Univ, Fac Sci, Wagga Wagga, NSW, Australia Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USABlanchard, Christopher L.论文数: 0 引用数: 0 h-index: 0机构: Charles Sturt Univ, Fac Sci, Wagga Wagga, NSW, Australia Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USAElsea, Sarah H.论文数: 0 引用数: 0 h-index: 0机构: Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USA Virginia Commonwealth Univ, Dept Pediat & Human Genet, Richmond, VA 23298 USA