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- [41] Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer familiesBMC Cancer, 19Rajendra Bahadur Shahi论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Sylvia De Brakeleer论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Ben Caljon论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Ingrid Pauwels论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Maryse Bonduelle论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Sofie Joris论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Christel Fontaine论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Marian Vanhoeij论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Sonia Van Dooren论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Erik Teugels论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)Jacques De Grève论文数: 0 引用数: 0 h-index: 0机构: Vrije Universiteit Brussel (VUB),Laboratory of Medical and Molecular Oncology (LMMO)
- [42] Detection of Novel Biallelic Causative Variants in COL7A1 Gene by Whole-Exome Sequencing, Resulting in Congenital Recessive Dystrophic Epidermolysis Bullosa in Three Unrelated FamiliesDIAGNOSTICS, 2022, 12 (07)Fozia, Fozia论文数: 0 引用数: 0 h-index: 0机构: Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, Pakistan Kohat Univ Sci & Technol KUST, Dept Biotechnol & Genet Engn, Kohat 26000, Khyber Pakhtunk, Pakistan Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanNazli, Rubina论文数: 0 引用数: 0 h-index: 0机构: Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, Pakistan Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanAlrashed, May Mohammed论文数: 0 引用数: 0 h-index: 0机构: King Saud Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Chair Med & Mol Genet Res, POB 10219, Riyadh 11433, Saudi Arabia Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanGhneim, Hazem K.论文数: 0 引用数: 0 h-index: 0机构: King Saud Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Chair Med & Mol Genet Res, POB 10219, Riyadh 11433, Saudi Arabia Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanUl Haq, Zia论文数: 0 引用数: 0 h-index: 0机构: Khyber Med Univ KMU, Inst Publ Hlth & Social Sci IPH & SS, Peshawar 25100, Khyber Pakhtunk, Pakistan Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanJabeen, Musarrat论文数: 0 引用数: 0 h-index: 0机构: KMU Inst Med Sci, Dept Gynaecol & Obstet, Kohat 26000, Khyber Pakhtunk, Pakistan Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanKhan, Sher Alam论文数: 0 引用数: 0 h-index: 0机构: Kohat Univ Sci & Technol KUST, Dept Biotechnol & Genet Engn, Kohat 26000, Khyber Pakhtunk, Pakistan Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanAhmad, Ijaz论文数: 0 引用数: 0 h-index: 0机构: Kohat Univ Sci & Technol KUST, Dept Chem, Kohat 26000, Khyber Pakhtunk, Pakistan Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanBourhia, Mohammed论文数: 0 引用数: 0 h-index: 0机构: Univ Hassan 2, Fac Med & Pharm, Lab Chem Biochem Nutr & Environm, Casablanca 20000, Morocco Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, PakistanAboul-Soud, Mourad A. M.论文数: 0 引用数: 0 h-index: 0机构: King Saud Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Chair Med & Mol Genet Res, POB 10219, Riyadh 11433, Saudi Arabia Khyber Med Univ KMU, Inst Basic Med Sci IBMS, Peshawar 25100, Khyber Pakhtunk, Pakistan
- [43] Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer familiesBMC CANCER, 2019, 19 (1)Shahi, Rajendra Bahadur论文数: 0 引用数: 0 h-index: 0机构: VUB, LMMO, Brussels, Belgium VUB, LMMO, Brussels, BelgiumDe Brakeleer, Sylvia论文数: 0 引用数: 0 h-index: 0机构: VUB, LMMO, Brussels, Belgium VUB, LMMO, Brussels, BelgiumCaljon, Ben论文数: 0 引用数: 0 h-index: 0机构: VUB, Brussels Interuniv Genom High Throughput Core BRI, Univ Ziekenhuis Brussel UZ Brussel, Brussels, Belgium VUB, LMMO, Brussels, BelgiumPauwels, Ingrid论文数: 0 引用数: 0 h-index: 0机构: Univ Ziekenhuis Brussel UZ Brussel, Familial Canc Clin, Oncol Ctr, Brussels, Belgium VUB, LMMO, Brussels, BelgiumBonduelle, Maryse论文数: 0 引用数: 0 h-index: 0机构: VUB, Univ Ziekenhuis Brussel UZ Brussel, Ctr Med Genet Reprod & Genet, Brussels, Belgium VUB, LMMO, Brussels, BelgiumJoris, Sofie论文数: 0 引用数: 0 h-index: 0机构: Univ Ziekenhuis Brussel UZ Brussel, Familial Canc Clin, Oncol Ctr, Brussels, Belgium VUB, LMMO, Brussels, BelgiumFontaine, Christel论文数: 0 引用数: 0 h-index: 0机构: Univ Ziekenhuis Brussel UZ Brussel, Breast Canc Clin, Oncol Ctr, Brussels, Belgium VUB, LMMO, Brussels, BelgiumVanhoeij, Marian论文数: 0 引用数: 0 h-index: 0机构: Univ Ziekenhuis Brussel UZ Brussel, Breast Canc Clin, Oncol Ctr, Brussels, Belgium VUB, LMMO, Brussels, BelgiumVan Dooren, Sonia论文数: 0 引用数: 0 h-index: 0机构: VUB, Brussels Interuniv Genom High Throughput Core BRI, Univ Ziekenhuis Brussel UZ Brussel, Brussels, Belgium VUB, Univ Ziekenhuis Brussel UZ Brussel, Ctr Med Genet Reprod & Genet, Brussels, Belgium VUB, LMMO, Brussels, BelgiumTeugels, Erik论文数: 0 引用数: 0 h-index: 0机构: VUB, LMMO, Brussels, Belgium Univ Ziekenhuis Brussel UZ Brussel, Familial Canc Clin, Oncol Ctr, Brussels, Belgium VUB, LMMO, Brussels, BelgiumDe Greve, Jacques论文数: 0 引用数: 0 h-index: 0机构: VUB, LMMO, Brussels, Belgium Univ Ziekenhuis Brussel UZ Brussel, Familial Canc Clin, Oncol Ctr, Brussels, Belgium VUB, LMMO, Brussels, Belgium
- [44] A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencingMOLECULAR GENETICS & GENOMIC MEDICINE, 2018, 6 (05): : 739 - 748Yang, Junli论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaWang, Qiong论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ Sci & Technol, Inst Biol & Med, QingLing St, Wuhan 430081, Hubei, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaZhuo, Qingcui论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaTian, Huiling论文数: 0 引用数: 0 h-index: 0机构: Linyi Women & Childrens Hosp, Children Rehabil Ctr, Linyi, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaLi, Wen论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaLuo, Fang论文数: 0 引用数: 0 h-index: 0机构: MyGenostics Inc, Beijing, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaZhang, Jinghui论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaBi, Dan论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaPeng, Jing论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ Sci & Technol, Inst Biol & Med, QingLing St, Wuhan 430081, Hubei, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaZhou, Dong论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R ChinaXin, Huawei论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ Sci & Technol, Inst Biol & Med, QingLing St, Wuhan 430081, Hubei, Peoples R China Linyi Univ, Sch Pharm, Linyi, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China
- [45] Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1 and BRCA2 VariantsGENES, 2022, 13 (04)Alenezi, Wejdan M.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada McGill Univ, Canc Res Program, Ctr Translat Biol, Res Inst,Hlth Ctr, Montreal, PQ H4A 3J1, Canada Taibah Univ, Dept Med Lab Technol, Medina 42353, Saudi Arabia McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaFierheller, Caitlin T.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada McGill Univ, Canc Res Program, Ctr Translat Biol, Res Inst,Hlth Ctr, Montreal, PQ H4A 3J1, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaRevil, Timothee论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada McGill Univ, McGill Genome Ctr, Montreal, PQ, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaSerruya, Corinne论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Canc Res Program, Ctr Translat Biol, Res Inst,Hlth Ctr, Montreal, PQ H4A 3J1, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaMes-Masson, Anne-Marie论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Dept Med, Montreal, PQ, Canada Univ Montreal, Inst Canc Montreal, Ctr Rech Ctr Hosp, Montreal, PQ H2X 0A9, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaFoulkes, William D.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada McGill Univ, Canc Res Program, Ctr Translat Biol, Res Inst,Hlth Ctr, Montreal, PQ H4A 3J1, Canada Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada McGill Univ, Dept Med Genet, Hlth Ctr, Montreal, PQ H3H 1P3, Canada McGill Univ, Dept Med, Montreal, PQ H4A 3J1, Canada McGill Univ, Gerald Bronfman Dept Oncol, Montreal, PQ H3A 1G5, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaProvencher, Diane论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Inst Canc Montreal, Ctr Rech Ctr Hosp, Montreal, PQ H2X 0A9, Canada Univ Montreal, Div Gynecol Oncol, Montreal, PQ H4A 3J1, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaEl Haffaf, Zaki论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Inst Canc Montreal, Ctr Rech Ctr Hosp, Montreal, PQ H2X 0A9, Canada Ctr Hosp Univ Montreal, Serv Med Genique, Montreal, PQ H2X 0A9, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaRagoussis, Jiannis论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada McGill Univ, McGill Genome Ctr, Montreal, PQ, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, CanadaTonin, Patricia N.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada McGill Univ, Canc Res Program, Ctr Translat Biol, Res Inst,Hlth Ctr, Montreal, PQ H4A 3J1, Canada McGill Univ, Dept Med, Montreal, PQ H4A 3J1, Canada McGill Univ, Dept Human Genet, Montreal, PQ H3A 0C7, Canada
- [46] An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencingAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (04) : 1080 - 1085Mackenroth, Luisa论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Inst Clin Genet, Fac Med Carl Gustav Carus, Dresden, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyFischer-Zirnsak, Bjoern论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyEgerer, Johannes论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyHecht, Jochen论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyKallinich, Tilmann论文数: 0 引用数: 0 h-index: 0机构: Charite, Dept Pediat Pneumol & Immunol, D-13353 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyStenzel, Werner论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Neuropathol, Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanySpors, Birgit论文数: 0 引用数: 0 h-index: 0机构: Charite, Dept Radiol, Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germanyvon Moers, Arpad论文数: 0 引用数: 0 h-index: 0机构: DRK Kliniken Westend, Childrens Hosp, Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyMundlos, Stefan论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyKornak, Uwe论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyGerhold, Kerstin论文数: 0 引用数: 0 h-index: 0机构: Charite, Dept Pediat Pneumol & Immunol, D-13353 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, GermanyHorn, Denise论文数: 0 引用数: 0 h-index: 0机构: Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany Charite, Inst Med & Human Genet, Augustenburger Pl 1, D-13353 Berlin, Germany
- [47] Identification of Two Variants c.2697A > C and c.3305A > C in USP7 by Analysis of Whole-Exome Sequencing in Chinese Patients with Hao-Fountain SyndromeGLOBAL MEDICAL GENETICS, 2024, 11 (01): : 13 - 19Sun, Mei论文数: 0 引用数: 0 h-index: 0机构: Tianjin Med Univ, Grad Coll, Tianjin, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaLi, Qing论文数: 0 引用数: 0 h-index: 0机构: Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Tianjin, Peoples R China Tianjin Univ, Childrens Hosp, Tianjin Childrens Hosp, Dept Neurol, Tianjin, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaZhang, Ying论文数: 0 引用数: 0 h-index: 0机构: Tianjin Med Univ, Grad Coll, Tianjin, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaCai, Yingzi论文数: 0 引用数: 0 h-index: 0机构: Tianjin Univ, Acad Med Engn & Translat Med, Tianjin, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaDong, Yan论文数: 0 引用数: 0 h-index: 0机构: Tianjin Med Univ, Grad Coll, Tianjin, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaShu, Jianbo论文数: 0 引用数: 0 h-index: 0机构: Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Tianjin, Peoples R China Tianjin Univ, Childrens Hosp, Tianjin Childrens Hosp, Tianjin Pediat Res Inst, Tianjin, Peoples R China Tianjin Childrens Hosp, Tianjin Key Lab Birth Defects Prevent & Treatment, Tianjin, Peoples R China Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Tianjin Pediat Res Inst, 238 Longyan Rd, Tianjin 300134, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaLi, Dong论文数: 0 引用数: 0 h-index: 0机构: Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Tianjin, Peoples R China Tianjin Univ, Childrens Hosp, Tianjin Childrens Hosp, Dept Neurol, Tianjin, Peoples R China Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Dept Neurol, 238 Longyan Rd, Tianjin 300134, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R ChinaCai, Chunquan论文数: 0 引用数: 0 h-index: 0机构: Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Tianjin, Peoples R China Tianjin Univ, Childrens Hosp, Tianjin Childrens Hosp, Tianjin Pediat Res Inst, Tianjin, Peoples R China Tianjin Childrens Hosp, Tianjin Key Lab Birth Defects Prevent & Treatment, Tianjin, Peoples R China Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Tianjin Pediat Res Inst, 238 Longyan Rd, Tianjin 300134, Peoples R China Tianjin Med Univ, Grad Coll, Tianjin, Peoples R China