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- [41] Whole-exome sequencing study reveals common copy number variants in protocadherin genes associated with childhood obesity in KoreansINTERNATIONAL JOURNAL OF OBESITY, 2017, 41 (04) : 660 - 663Moon, S.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaHwang, M. Y.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaJang, H. B.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Biomed Sci, Div Metab Dis, Chungcheongbuk Do, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaHan, S.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaKim, Y. J.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaHwang, J-Y论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaLee, H-J论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Biomed Sci, Div Metab Dis, Chungcheongbuk Do, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaPark, S. I.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Biomed Sci, Div Metab Dis, Chungcheongbuk Do, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaSong, J.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Biomed Sci, Div Metab Dis, Chungcheongbuk Do, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South KoreaKim, B-J论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, 187 Osongsaengmyeong 2Ro Osong Eup, Cheongju 28159, Chungcheongbuk, South Korea
- [42] Whole exome sequencing reveals novel variants associated with diminished ovarian reserve in young womenFRONTIERS IN GENETICS, 2023, 14Li, Na论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaXu, Wanxue论文数: 0 引用数: 0 h-index: 0机构: Peking Univ Third Hosp, Ctr Reprod Med, Dept Obstet & Gynecol, Beijing, Peoples R China Peking Univ Third Hosp, Ctr Reprod Med, Dept Obstet & Gynecol, Beijing, Peoples R China Minist Educ, Key Lab Assisted Reprod, Beijing, Peoples R China Beijing Key Lab Reprod Endocrinol & Assisted Repro, Beijing, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaLiu, Huimin论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaZhou, Rui论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaZou, Siqi论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaWang, Shiqing论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaLi, Siyu论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaYang, Zexin论文数: 0 引用数: 0 h-index: 0机构: Tianjin Med Univ, Grad Sch, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaPiao, Yongjun论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Tianjin Cent Hosp Obstet & Gynecol, Dept Ctr Reprod Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R ChinaZhang, Yunshan论文数: 0 引用数: 0 h-index: 0机构: Nankai Univ, Sch Med, Tianjin, Peoples R China Tianjin Cent Hosp Obstet & Gynecol, Dept Ctr Reprod Med, Tianjin, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R China
- [43] Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited RetinopathiesScientific Reports, 5Avigail Beryozkin论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyElia Shevah论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyAdva Kimchi论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyLiliana Mizrahi-Meissonnier论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologySamer Khateb论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyRinki Ratnapriya论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyCsilla H. Lazar论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyAnat Blumenfeld论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyTamar Ben-Yosef论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyYitzhak Hemo论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyJacob Pe’er论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyEduard Averbuch论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyMichal Sagi论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyAlexis Boleda论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyLinn Gieser论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyAbraham Zlotogorski论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyTzipora Falik-Zaccai论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyOla Alimi-Kasem论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologySamuel G. Jacobson论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyItay Chowers论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyAnand Swaroop论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyEyal Banin论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of OphthalmologyDror Sharon论文数: 0 引用数: 0 h-index: 0机构: Hadassah-Hebrew University Medical Center,Departments of Ophthalmology
- [44] Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited RetinopathiesSCIENTIFIC REPORTS, 2015, 5Beryozkin, Avigail论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelShevah, Elia论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelKimchi, Adva论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelMizrahi-Meissonnier, Liliana论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelKhateb, Samer论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelRatnapriya, Rinki论文数: 0 引用数: 0 h-index: 0机构: NEI, Neurobiol Neurodegenerat & Repair Lab, NIH, Bethesda, MD 20892 USA Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelLazar, Csilla H.论文数: 0 引用数: 0 h-index: 0机构: NEI, Neurobiol Neurodegenerat & Repair Lab, NIH, Bethesda, MD 20892 USA Univ Babes Bolyai, Mol Biol Ctr, Interdisciplinary Res Inst Bionano Sci, Cluj Napoca 400271, Romania Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelBlumenfeld, Anat论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelBen-Yosef, Tamar论文数: 0 引用数: 0 h-index: 0机构: Technion Israel Inst Technol, Rappaport Fac Med, Haifa, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelHemo, Yitzhak论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelPe'er, Jacob论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelAverbuch, Eduard论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelSagi, Michal论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Human Genet, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelBoleda, Alexis论文数: 0 引用数: 0 h-index: 0机构: NEI, Neurobiol Neurodegenerat & Repair Lab, NIH, Bethesda, MD 20892 USA Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelGieser, Linn论文数: 0 引用数: 0 h-index: 0机构: NEI, Neurobiol Neurodegenerat & Repair Lab, NIH, Bethesda, MD 20892 USA Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelZlotogorski, Abraham论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dermatol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelFalik-Zaccai, Tzipora论文数: 0 引用数: 0 h-index: 0机构: Inst Human Genet, Galilee Med Ctr, Nahariyya, Israel Galilee Fac Med, Bar Ilan, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelAlimi-Kasem, Ola论文数: 0 引用数: 0 h-index: 0机构: Haemek Hosp, Afula, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelJacobson, Samuel G.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Scheie Eye Inst, Dept Ophthalmol, Philadelphia, PA 19104 USA Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelChowers, Itay论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelSwaroop, Anand论文数: 0 引用数: 0 h-index: 0机构: NEI, Neurobiol Neurodegenerat & Repair Lab, NIH, Bethesda, MD 20892 USA Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelBanin, Eyal论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, IsraelSharon, Dror论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Dept Ophthalmol, Jerusalem, Israel
- [45] Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiencyJOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2022, 39 (03) : 695 - 710Turkyilmaz, Ayberk论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, Turkey论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Geckinli, Bilgen Bilge论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyPolat, Hamza论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyGokcu, Mehmet论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyKarakaya, Taner论文数: 0 引用数: 0 h-index: 0机构: Isparta City Hosp, Dept Med Genet, Isparta, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyCebi, Alper Han论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeySoylemez, Mehmet Ali论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyGuney, Ahmet Ilter论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyAta, Pinar论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, TurkeyArman, Ahmet论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, Istanbul, Turkey Karadeniz Tech Univ, Sch Med, Dept Med Genet, Trabzon, Turkey
- [46] Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeHYPERTENSION, 2018, 71 (04) : 691 - 699Warejko, Jillian K.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Yale Sch Med, Yale New Haven Childrens Hosp, Dept Pediat, New Haven, CT USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USASchueler, Markus论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USAVivante, Asaf论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Sheba Med Ctr, Talpiot Med Leadership Program, Tel Hashomer, Israel Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USATan, Weizhen论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USADaga, Ankana论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USALawson, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USABraun, Daniela A.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USAShril, Shirlee论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USAAmann, Kassaundra论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Dept Med, Boston, MA USASomers, Michael J. 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- [47] Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiencyJournal of Assisted Reproduction and Genetics, 2022, 39 : 695 - 710Ayberk Turkyilmaz论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineCeren Alavanda论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineEsra Arslan Ates论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineBilgen Bilge Geckinli论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineHamza Polat论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineMehmet Gokcu论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineTaner Karakaya论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineAlper Han Cebi论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineMehmet Ali Soylemez论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineAhmet İlter Guney论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicinePinar Ata论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of MedicineAhmet Arman论文数: 0 引用数: 0 h-index: 0机构: Karadeniz Technical University,Department of Medical Genetics, School of Medicine
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