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- [31] Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomaliesEUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2020, 251 : 119 - 124Chen, Min论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaChen, Jingsi论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaWang, Chunli论文数: 0 引用数: 0 h-index: 0机构: AmCare Genom Lab, Guangzhou 510300, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaChen, Fei论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaXie, Yinong论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaLi, Yufan论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaLi, Nan论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaWang, Jing论文数: 0 引用数: 0 h-index: 0机构: AmCare Genom Lab, Guangzhou 510300, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaZhang, Victor Wei论文数: 0 引用数: 0 h-index: 0机构: AmCare Genom Lab, Guangzhou 510300, Guangdong, Peoples R China Baylor Coll Med, Dept Human & Mol Genet, Houston, TX 77030 USA Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R ChinaChen, Dunjin论文数: 0 引用数: 0 h-index: 0机构: Obstet Ea Gynecol Inst Guangzhou, Guangzhou 510150, Peoples R China Med Ctr Crit Pregnant Women Guangzhou, Guangzhou 510150, Peoples R China Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China Key Lab Reprod & Genet Guangdong Higher Educ Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Dept Fetal Med & Prenatal Diag, Affiliated Hosp 3, Guangzhou 510150, Peoples R China
- [32] Unveiling the potential: evaluating prenatal genetic diagnosis through exome trio sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1599 - 1600Asensio-Landa, Victor论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainSanchez, Sara论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainMartorell, Rosa论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Servicio Ginecol & Obstetricia, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainSuner, Damian Heine论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainTorres-Juan, Laura论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainSantos-Simarro, Fernando论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainPaso, Maria Garcia-De论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainAvella-Klaassen, Susana Renee论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainPrado-Farnos, Maria Carmen论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainVila, Maria论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Servicio Ginecol & Obstetricia, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainAlegre, Andrea论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Servicio Ginecol & Obstetricia, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spainde Gopegui, Rosa Ruiz论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Servicio Ginecol & Obstetricia, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainTubau, Albert论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Llatzer, Servicio Ginecol & Obstetricia, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, SpainMartinez, Iciar论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain Hosp Univ Son Espases, Unidad Diagnostico Mole & Genet Clin, Palma De Mallorca, Spain
- [33] Application of Whole-Exome Sequencing in the Genetic Diagnosis of Prenatal Ultrasound AbnormalitiesBRITISH JOURNAL OF HOSPITAL MEDICINE, 2024, 85 (12)Qin, Lili论文数: 0 引用数: 0 h-index: 0机构: Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R China Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R ChinaLiu, Datong论文数: 0 引用数: 0 h-index: 0机构: Jining Med Coll, Clin Med Sch, Jining, Shandong, Peoples R China Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R ChinaWang, Xuanyi论文数: 0 引用数: 0 h-index: 0机构: GenPhysio, Nutr Counselling Dept, Southport, Qld, Australia Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R ChinaXia, Yu论文数: 0 引用数: 0 h-index: 0机构: Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R China Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R ChinaSun, Meiling论文数: 0 引用数: 0 h-index: 0机构: Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R China Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R ChinaChen, Huizi论文数: 0 引用数: 0 h-index: 0机构: Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R China Rizhao Peoples Hosp, Dept Obstet & Gynecol, Rizhao, Shandong, Peoples R China
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- [35] Multidisciplinary committee's impact on prenatal whole exome sequencing variant interpretationAMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2023, 228 (01) : S345 - S345Micke, Kestutis论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Aurora, CO USA Univ Colorado, Aurora, CO USAElfman, Hannah论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Aurora, CO USA Univ Colorado, Aurora, CO USAReynolds, Regina论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Aurora, CO USA Univ Colorado, Aurora, CO USAAustin, Larson论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Aurora, CO USA Univ Colorado, Aurora, CO USAShawn, McCandless论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Aurora, CO USA Univ Colorado, Aurora, CO USAZaretsky, Michael V.论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado, Sch Med, Aurora, CO USA Univ Colorado, Aurora, CO USA
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- [38] Whole-exome sequencing enables rapid and prenatal diagnosis of inherited skin disordersBMC MEDICAL GENOMICS, 2023, 16 (01)Xintong, Zhu论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R China Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R ChinaKexin, Zhang论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Southwest Hosp, Dept Dermatol, 30 Gaotanyan St, Chongqing 400038, Peoples R China Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R ChinaJunwen, Wang论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R China Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R ChinaZiyi, Wang论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R China Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R ChinaNa, Luo论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Southwest Hosp, Dept Dermatol, 30 Gaotanyan St, Chongqing 400038, Peoples R China Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R ChinaHong, Guo论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R China Army Med Univ, Coll Basic Med Sci, Dept Med Genet, 30 Gaotanyan St, Chongqing 400038, Peoples R China
- [39] Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic toolFRONTIERS IN GENETICS, 2023, 14Tran Mau-Them, Frederic论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceDelanne, Julian论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceDenomme-Pichon, Anne-Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSafraou, Hana论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceVitobello, Antonio论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceGarde, Aurore论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceNambot, Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBourgon, Nicolas论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceRacine, Caroline论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSorlin, Arthur论文数: 0 引用数: 0 h-index: 0机构: INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceMoutton, Sebastien论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceMarle, Nathalie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genet Chromosom & Mol, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceRousseau, Thierry论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Dijon Bourgogne, Serv Gynecol Obstet Med Foetale & Sterilite Conju, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSagot, Paul论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Dijon Bourgogne, Serv Gynecol Obstet Med Foetale & Sterilite Conju, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSimon, Emmanuel论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Dijon Bourgogne, Serv Gynecol Obstet Med Foetale & Sterilite Conju, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceVincent-Delorme, Catherine论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBoute, Odile论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceColson, Cindy论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FrancePetit, Florence论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceLegendre, Marine论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceNaudion, Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceRooryck, Caroline论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceProuteau, Clement论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceColin, Estelle论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France 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