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- [1] Identification of a novel frameshift variation in ANKRD11: a case report of KBG syndromeFRONTIERS IN GENETICS, 2025, 15Shao, Qing论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaJiang, Qiang论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaLuo, Yuqi论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaMeng, Yimei论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaTian, Guoyu论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R ChinaYin, Xiao论文数: 0 引用数: 0 h-index: 0机构: Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China Shandong First Univ, Affiliated Cent Hosp, Dept Endocrinol & Metab Dis, Jinan, Peoples R China
- [2] Audiological findings in a de novo mutation of ANKRD11 gene in KBG syndrome: Report of a case and review of the literatureINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2017, 103 : 109 - 112Bianchi, Pier Marco论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, Italy Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, ItalyBianchi, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Sapienza Univ, ENT Clin Med & Psychol, NESMOS Dept, Rome, Italy Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, ItalyDigilio, Maria Cristina论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Paediat Hosp, Sci Res Inst, Genet & Rare Dis Res Div, I-00100 Rome, Italy Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, ItalyTucci, Filippo Maria论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, Italy Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, ItalySitzia, Emanuela论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, Italy Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, ItalyDe Vincentiis, Giovanni Carlo论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, Italy Bambino Gesu Paediat Hosp, Sci Res Inst, Otorhinolaryngol Unit, Surg Dept, I-00100 Rome, Italy
- [3] Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature ReviewFRONTIERS IN GENETICS, 2020, 11Kim, Su Jin论文数: 0 引用数: 0 h-index: 0机构: Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South Korea Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South Korea论文数: 引用数: h-index:机构:Park, Ji Sun论文数: 0 引用数: 0 h-index: 0机构: Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South Korea Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South KoreaKwon, Dae Gyu论文数: 0 引用数: 0 h-index: 0机构: Inha Univ, Coll Med, Inha Univ Hosp, Dept Orthopaed Surg, Incheon, South Korea Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South KoreaLee, Jeong-Seop论文数: 0 引用数: 0 h-index: 0机构: Inha Univ, Inha Univ Hosp, Coll Med, Dept Psychiat, Incheon, South Korea Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South Korea论文数: 引用数: h-index:机构:Lee, Ji Eun论文数: 0 引用数: 0 h-index: 0机构: Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South Korea Inha Univ, Coll Med, Inha Univ Hosp, Dept Pediat, Incheon, South Korea
- [4] Characterization of ANKRD11 mutations in humans and mice related to KBG syndromeHuman Genetics, 2015, 134 : 181 - 190Katherina Walz论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsDevon Cohen论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsPaul M. Neilsen论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsJoseph Foster论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsFrancesco Brancati论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsKorcan Demir论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsRichard Fisher论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsMichelle Moffat论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsNienke E. Verbeek论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsKathrine Bjørgo论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsAdriana Lo Castro论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsPaolo Curatolo论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsGiuseppe Novelli论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsClemer Abad论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsCao Lei论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsLily Zhang论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsOscar Diaz-Horta论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsJuan I. Young论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsDavid F. Callen论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GenomicsMustafa Tekin论文数: 0 引用数: 0 h-index: 0机构: Miller School of Medicine,Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics
- [5] Characterization of ANKRD11 mutations in humans and mice related to KBG syndromeHUMAN GENETICS, 2015, 134 (02) : 181 - 190Walz, Katherina论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dept Med, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USACohen, Devon论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USANeilsen, Paul M.论文数: 0 引用数: 0 h-index: 0机构: Swinburne Univ Technol Sarawak Campus, Kuching, Sarawak, Malaysia Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAFoster, Joseph, II论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USABrancati, Francesco论文数: 0 引用数: 0 h-index: 0机构: Gabriele DAnnunzio Univ, Dept Med Oral & Biotechnol Sci, I-66100 Chieti, Italy Policlin Tor Vergata Univ Hosp, Med Genet Unit, I-00133 Rome, Italy Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USADemir, Korcan论文数: 0 引用数: 0 h-index: 0机构: Dokuz Eylul Univ, Fac Med, Div Pediat Endocrinol, TR-35340 Izmir, Turkey Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAFisher, Richard论文数: 0 引用数: 0 h-index: 0机构: James Cook Univ Hosp, Northern Genet Serv, Teesside Genet Unit, Middlesbrough TS4 3BW, Cleveland, England Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAMoffat, Michelle论文数: 0 引用数: 0 h-index: 0机构: Newcastle Dent Hosp & Sch, Dept Paediat Dent, Newcastle Upon Tyne NE2 4AZ, Tyne & Wear, England Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAVerbeek, Nienke E.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Med Genet, NL-3584 EA Utrecht, Netherlands Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USABjorgo, Kathrine论文数: 0 引用数: 0 h-index: 0机构: Oslo Univ Hosp, Dept Med Genet, N-0450 Oslo, Norway Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USALo Castro, Adriana论文数: 0 引用数: 0 h-index: 0机构: Univ Roma Tor Vergata, Dept Neurosci, Pediat Neurol & Psychiat Unit, I-00165 Rome, Italy Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USACuratolo, Paolo论文数: 0 引用数: 0 h-index: 0机构: Univ Roma Tor Vergata, Dept Neurosci, Pediat Neurol & Psychiat Unit, I-00165 Rome, Italy Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USANovelli, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Policlin Tor Vergata Univ Hosp, Med Genet Unit, I-00133 Rome, Italy Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAAbad, Clemer论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USALei, Cao论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAZhang, Lily论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USADiaz-Horta, Oscar论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USAYoung, Juan I.论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USACallen, David F.论文数: 0 引用数: 0 h-index: 0机构: Swinburne Univ Technol Sarawak Campus, Kuching, Sarawak, Malaysia Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USATekin, Mustafa论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA
- [6] Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 geneActa Neurologica Belgica, 2015, 115 : 779 - 782Debopam Samanta论文数: 0 引用数: 0 h-index: 0机构: University of Arkansas for Medical Sciences,Division of Child NeurologyErin Willis论文数: 0 引用数: 0 h-index: 0机构: University of Arkansas for Medical Sciences,Division of Child Neurology
- [7] Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 geneACTA NEUROLOGICA BELGICA, 2015, 115 (04) : 779 - 782Samanta, Debopam论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USAWillis, Erin论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Div Child Neurol, Little Rock, AR 72205 USA
- [8] Enostosis in a patient with KBG syndrome caused by a novel missense ANKRD11 variantCLINICAL DYSMORPHOLOGY, 2022, 31 (03) : 153 - 156Geckinli, Bilgen Bilge论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Yildirim, Ozlem论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Inst Sci, Dept Mol Biol & Genet, Istanbul, Turkey Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, TurkeyArman, Ahmet论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey Marmara Univ, Sch Med, Dept Med Genet, TR-34890 Istanbul, Turkey
- [9] Identification of Two Novel ANKRD11 Mutations: Highlighting Incomplete Penetrance in KBG SyndromeANNALS OF LABORATORY MEDICINE, 2024, 44 (01) : 110 - 117Amllal, Nada论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco Natl Inst Hlth, Dept Med Genet, Ibn Batouta Ave, nb 27, Rabat 10090, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoElalaoui, Siham Chafai论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco Med Genet Unit, CHU Ibn Sina, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoZerkaoui, Maria论文数: 0 引用数: 0 h-index: 0机构: Med Genet Unit, CHU Ibn Sina, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoChiguer, Amal论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco Natl Inst Hlth, Dept Med Genet, Ibn Batouta Ave, nb 27, Rabat 10090, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoAfif, Lamia论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco Natl Inst Hlth, Dept Med Genet, Ibn Batouta Ave, nb 27, Rabat 10090, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoIzgua, Amal Thimou论文数: 0 引用数: 0 h-index: 0机构: CHU IBN SINA, Ctr Consultat & External Explorat, HER, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoSefiani, Abdelaziz论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco Natl Inst Hlth, Dept Med Genet, Ibn Batouta Ave, nb 27, Rabat 10090, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, MoroccoLyahyai, Jaber论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Genom Ctr Human Pathol, Res Team Genom & Mol Epidemiol Genet Dis, Rabat, Morocco
- [10] Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndromeHELIYON, 2024, 10 (06)Wei, Shuoshuo论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Med Res Ctr, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaLi, Yanying论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Chinese Res Ctr Behav Med Growth & Dev, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaYang, Wanling论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaChen, Shuxiong论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Med Res Ctr, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaLiu, Fupeng论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Med Res Ctr, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaZhang, Mei论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Chinese Res Ctr Behav Med Growth & Dev, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaBan, Bo论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Med Res Ctr, Jining, Peoples R China Chinese Res Ctr Behav Med Growth & Dev, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R ChinaHe, Dongye论文数: 0 引用数: 0 h-index: 0机构: Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Med Res Ctr, Jining, Peoples R China Jining Med Univ, Affiliated Hosp, Dept Endocrinol Genet & Metab, Jining, Peoples R China