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- [41] Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome)PRENATAL DIAGNOSIS, 2023, 43 (06) : 734 - 745Courdier, Cecile论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceBoudjarane, John论文数: 0 引用数: 0 h-index: 0机构: Hop Timone Enfants, AP HM, Dept Genet Medicale, Lab Cytogenet, Marseille, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceMalan, Valerie论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Serv Medecine Genomique Malad Rares, Paris, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceMuti, Christine论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Versailles, Unite Genet, Versailles, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceSperelakis-Beedham, Brian论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Versailles, Unite Genet, Versailles, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Serv Genet Clin, Rennes, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceJaillard, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Serv Cytogenet & Biol Cellulaire, Rennes, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceQuelin, Chloe论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Serv Genet Clin, Rennes, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceLe Caignec, Cedric论文数: 0 引用数: 0 h-index: 0机构: CHU Toulouse, Hop Purpan, Serv Genet Med, Toulouse, France CHU Bordeaux, Serv Genet Med, Bordeaux, FrancePatat, Olivier论文数: 0 引用数: 0 h-index: 0机构: CHU Toulouse, Hop Purpan, Serv Genet Med, Toulouse, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceDubucs, Charlotte论文数: 0 引用数: 0 h-index: 0机构: CHU Toulouse, Hop Purpan, Serv Genet Med, Toulouse, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceJulia, Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Toulouse, Hop Purpan, Serv Genet Med, Toulouse, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceSchluth-Bolard, Caroline论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Ctr Biol & Pathol Est, Serv Genet, Lab Cytogenet Constitut, Bron, France Univ Strasbourg, Hop Univ Strasbourg, Inst Genet Medicale Alsace, Lab Diagnost Genet, Strasbourg, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceGoumy, Carole论文数: 0 引用数: 0 h-index: 0机构: CHU Estaing, Serv Cytogenet Med, Clermont Ferrand, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceRedon, Sylvia论文数: 0 引用数: 0 h-index: 0机构: CHRU Morvan, Lab Genet Mol & dhistocompatibil, INSERM U1078, Brest, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceGaillard, Jean-Baptiste论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Unite Genet Chromos, Montpellier, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceHuynh, Minh Tuan论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Lab Genet Med, Nantes, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceDupont, Celine论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Dept Genet, Unite fonct Cytogenet, Paris, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceTabet, Anne-Claude论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Dept Genet, Unite fonct Cytogenet, Paris, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceCogan, Guillaume论文数: 0 引用数: 0 h-index: 0机构: Univ Picardie Jules Verne, Ctr Univ Rech St, HEMATIM UR4666, Amiens, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceVialard, Francois论文数: 0 引用数: 0 h-index: 0机构: CHI Poissy St Germain En Laye, Dept Genet, Lab Biol Med, Poissy, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceDard, Rodolphe论文数: 0 引用数: 0 h-index: 0机构: CHI Poissy St Germain En Laye, Dept Genet, Lab Biol Med, Poissy, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceJedraszak, Guillaume论文数: 0 引用数: 0 h-index: 0机构: CHU Amiens, Lab Genet Constitut, Amiens, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceJobic, Florence论文数: 0 引用数: 0 h-index: 0机构: CHU Amiens, Serv Genet Clin & Oncogenet, Amiens, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceLefebvre, Mathilde论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, Serv Foetopathol, Paris, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceQuenum, Genevieve论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, Lab Cytogenet, Paris, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceInai, Saori论文数: 0 引用数: 0 h-index: 0机构: CH Libourne, Serv Gynecol, Libourne, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceRama, Melanie论文数: 0 引用数: 0 h-index: 0机构: CHRU Lille, Hop Jeanne Flandre, Inst Genet Med, Lille, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceSauvestre, Fanny论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Pathol, Unite Faetopathol, Bordeaux, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceCoatleven, Frederic论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Gynecol Obstet, Bordeaux, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceThomas, Julie论文数: 0 引用数: 0 h-index: 0机构: Hop Haut Leveque, Serv Malad Cardiovasc Congenitales, Bordeaux, France CHU Bordeaux, Serv Genet Med, Bordeaux, FranceRooryck, Caroline论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France Univ Bordeaux, Malad Rares Genet & Metab MRGM, INSERM U1211, Bordeaux, France CHU Bordeaux, Serv Genet Med, Grp Hosp Pellegrin, Pl Amelie Raba Leon, F-33076 Bordeaux, France CHU Bordeaux, Serv Genet Med, Bordeaux, France
- [42] Atypical deletion of Williams-Beuren syndrome reveals the mechanism of neurodevelopmental disordersBMC MEDICAL GENOMICS, 2022, 15 (01)Zhou, Jianrong论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Prov Key Lab South China Struct Heart D, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaZheng, Ying论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Nutr, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaLiang, Guiying论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Phys Therapy & Rehabil, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaXu, Xiaoli论文数: 0 引用数: 0 h-index: 0机构: Gen Hosp Cent Theater Command, Dept Endocrinol, Wuhan, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaLiu, Jian论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaChen, Shaoxian论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Prov Key Lab South China Struct Heart D, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Res Dept Med Sci, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaGe, Tongkai论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaWen, Pengju论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Res Dept Med Sci, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaZhang, Yong论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaLiu, Xiaoqing论文数: 0 引用数: 0 h-index: 0机构: Guangdong Prov Peoples Hosp, Div Epidemiol, Guangzhou, Peoples R China Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaZhuang, Jian论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Prov Key Lab South China Struct Heart D, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaWu, Yueheng论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Prov Key Lab South China Struct Heart D, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Phys Therapy & Rehabil, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R ChinaChen, Jimei论文数: 0 引用数: 0 h-index: 0机构: Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Prov Key Lab South China Struct Heart D, Guangzhou, Peoples R China Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Cardiovasc Surg, Guangdong Cardiovasc Inst, Guangzhou, Peoples R China
- [43] Characterization of the Williams syndrome deletion region on chromosome 7q11.23.AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A39 - A39Osborne, LR论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaSoder, S论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaHerbrick, JA论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaPober, B论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaCosta, T论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaShi, XM论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaHeng, HHQ论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaGreavette, TF论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaScherer, SW论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, CanadaTsui, LC论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, Canada
- [44] 7q11.23 deletion in patients with suspected Williams syndrome: a FISH analysis of 30 casesEUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 84 - 84Criado, B论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, PortugalFernandes, R论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, PortugalLima, MR论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, PortugalMota, CR论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, PortugalFortuna, AM论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, PortugalSaraiva, J论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, PortugalCastedo, S论文数: 0 引用数: 0 h-index: 0机构: IPATIMUP, Unidade Patol, Porto, Portugal
- [45] Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23BRAIN & DEVELOPMENT, 2017, 39 (02): : 145 - 153Muramatsu, Yukako论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Inst Dev Res, Dept Functioning Sci, 713-8 Kamiya Cho, Kasugai, Aichi 4800392, Japan Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi, Japan Aichi Human Serv Ctr, Inst Dev Res, Dept Functioning Sci, 713-8 Kamiya Cho, Kasugai, Aichi 4800392, JapanTokita, Yoshihito论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Inst Dev Res, Dept Perinatol, Kasugai, Aichi, Japan Aichi Human Serv Ctr, Inst Dev Res, Dept Functioning Sci, 713-8 Kamiya Cho, Kasugai, Aichi 4800392, JapanMizuno, Seiji论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Cent Hosp, Dept Pediat, Kasugai, Aichi, Japan Aichi Human Serv Ctr, Inst Dev Res, Dept Functioning Sci, 713-8 Kamiya Cho, Kasugai, Aichi 4800392, JapanNakamura, Miho论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Inst Dev Res, Dept Functioning Sci, 713-8 Kamiya Cho, Kasugai, Aichi 4800392, Japan Aichi Human Serv Ctr, Inst Dev Res, Dept Functioning Sci, 713-8 Kamiya Cho, Kasugai, Aichi 4800392, Japan
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- [47] Transcriptomic analysis of hiPSC-derived neurons from patients with Williams Beuren Syndrome and 7q11.23 microduplication syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 502 - 502Ugartondo, Nerea论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, Spain Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, SpainMartin-Mur, Beatriz论文数: 0 引用数: 0 h-index: 0机构: Barcelona Inst Sci & Technol BIST, Ctr Genom Regulat CRG, CNAG CRG, Barcelona, Spain Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, SpainSantamaria Canas, Mario论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, Spain Hosp Mar Med Res Inst IMIM UPF, Neurogen Grp, Res Programme Biomed Informat GRIB, MELIS, Barcelona, Spain Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, SpainBlasco-Fornies, Helena论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, Spain Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, SpainEsteve Codina, Anna论文数: 0 引用数: 0 h-index: 0机构: Barcelona Inst Sci & Technol BIST, Ctr Genom Regulat CRG, CNAG CRG, Barcelona, Spain Univ Pompeu Fabra UPF, Barcelona, Spain Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, SpainCorominas, Roser论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Barcelona, Spain Inst Biomed Univ Barcelona IBUB, Barcelona, Spain Inst Recerca St Joan Deu IRSJD, Barcelona, Spain Univ Barcelona, Dept Genet Microbiol & Stat, Barcelona, Spain
- [48] Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams-Beuren Region by Comparative GenomicsGENES, 2021, 12 (10)Cupaioli, Francesca Anna论文数: 0 引用数: 0 h-index: 0机构: Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, Italy Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, Italy论文数: 引用数: h-index:机构:Mencarelli, Maria Antonietta论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, ItalyPerticaroli, Valentina论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, ItalyFilippini, Virginia论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, ItalyMari, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, Italy论文数: 引用数: h-index:机构:Mezzelani, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, Italy Italian Natl Res Council, Inst Biomed Technol, Via Fratelli Cervi 93, I-20090 Segrate, Italy
- [49] Deletion of a small fragment of chromosome 7q11.23 containing ELN gene may be responsible for supravalvular aortic stenosis with pulmonary stenosis and no other features of Williams syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 165 - 166Bonda, W.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandBernatowicz, K.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Genet & Pathol, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandKashyap, A.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Genet & Pathol, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandKossowski, M.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandStudniak, E.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandRylow, M.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandWleczyk, C.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandBryskiewicz, M.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandPietrzak, J.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, PolandZajaczek, S.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Genet & Pathol, Szczecin, Poland Pomeranian Med Univ, Dept Lab Diagnost, Cytogenet Unit, Szczecin, Poland
- [50] Williams-Beuren syndrome in a family with a cytogenetically balanced t(7;16)(q11.23;q12.1)CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 146 - 147Duba, HC论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, AustriaNeyer, M论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, AustriaMann, C论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, AustriaDoll, A论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, AustriaErdel, M论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, AustriaHammerer, I论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, AustriaUtermann, G论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, Austria