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- [31] Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2020, 182 (10) : 2333 - 2344Murakami, Hiroaki论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanTsurusaki, Yoshinori论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanEnomoto, Keisuke论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKuroda, Yukiko论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanYokoi, Takayuki论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanFuruya, Noritaka论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanYoshihashi, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanMinatogawa, Mari论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanAbe-Hatano, Chihiro论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanOhashi, Ikuko论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanNishimura, Naoto论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKumaki, Tatsuro论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanEnomoto, Yumi论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanNaruto, Takuya论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanIwasaki, Fuminori论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Hematol Oncol, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanHarada, Noriaki论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Dept Clin Lab, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanIshikawa, Aki论文数: 0 引用数: 0 h-index: 0机构: Sapporo Med Univ, Dept Med Genet & Genom, Sch Med, Sapporo, Hokkaido, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKawame, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Grad Sch Med, Sendai, Miyagi, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanSameshima, Kiyoko论文数: 0 引用数: 0 h-index: 0机构: Gunma Childrens Med Ctr, Div Med Genet, Gunma, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanYamaguchi, Yu论文数: 0 引用数: 0 h-index: 0机构: Gunma Childrens Med Ctr, Div Med Genet, Gunma, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKobayashi, Masahisa论文数: 0 引用数: 0 h-index: 0机构: Jikei Univ, Dept Pediat, Sch Med, Tokyo, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanTominaga, Makiko论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Northern Yokohama Hosp, Childrens Med Ctr, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanIshikiriyama, Satoshi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Childrens Hosp, Div Clin Genet & Cytogenet, Shizuoka, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanTanaka, Toshiaki论文数: 0 引用数: 0 h-index: 0机构: Tanaka Growth Clin, Tokyo, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanSuzumura, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Dokkyo Med Univ, Dept Pediat, Mibu, Tochigi, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanNinomiya, Shinsuke论文数: 0 引用数: 0 h-index: 0机构: Kurashiki Cent Hosp, Dept Clin Genet, Kurashiki, Okayama, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKondo, Akane论文数: 0 引用数: 0 h-index: 0机构: Shikoku Med Ctr Children & Adults, Dept Gynecol, Zentsuji, Kagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKaname, Tadashi论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Child Hlth & Dev, Dept Genome Med, Tokyo, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKosaki, Kenjiro论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Ctr Med Genet, Tokyo, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanMasuno, Mitsuo论文数: 0 引用数: 0 h-index: 0机构: Kawasaki Univ Med Welf, Grad Sch Hlth & Welf, Genet Counseling Program, Kurashiki, Okayama, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKuroki, Yoshikazu论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, JapanKurosawa, Kenji论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan
- [32] A NOVEL MUTATION IN A PRIMARY IMMUNODEFICIENCY PATIENT REVEALING KABUKI SYNDROMEANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2016, 117 (05) : S86 - S86Mehta, M.论文数: 0 引用数: 0 h-index: 0Kobrynski, L.论文数: 0 引用数: 0 h-index: 0Shih, J.论文数: 0 引用数: 0 h-index: 0
- [33] A novel de novo mutation involving the MLL2 gene in a Kabuki syndrome patient presenting with seizuresTURKISH JOURNAL OF PEDIATRICS, 2016, 58 (01) : 97 - 100Bekircan-Kurt, Can Ebru论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Pediat, Dept Neurol, Ankara, Turkey Hacettepe Univ, Fac Med, Dept Pediat, Dept Neurol, Ankara, Turkey论文数: 引用数: h-index:机构:Boduroglu, Koray论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Pediat, Div Pediat Genet, Ankara, Turkey Hacettepe Univ, Fac Med, Dept Pediat, Dept Neurol, Ankara, TurkeyDericioglu, Nese论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Pediat, Dept Neurol, Ankara, Turkey Hacettepe Univ, Fac Med, Dept Pediat, Dept Neurol, Ankara, Turkey
- [34] De Novo Exonic Deletion of KDM6A in a Chinese Girl with Kabuki Syndrome: A Case Report and Brief Literature ReviewAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (06) : 1613 - 1621Yang, Pu论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaTan, Hu论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaXia, Yan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaYu, Qian论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp 2, Dept Haematol, Changsha, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaWei, Xianda论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaGuo, Ruolan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaPeng, Ying论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China论文数: 引用数: h-index:机构:Li, Haoxian论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaMei, Libin论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaHuang, Yanru论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaLiang, Desheng论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R ChinaWu, Lingqian论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China Cent S Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China
- [35] Five Novel Variants of KMT2D/KDM6A Found in Seven Chinese Patients with Kabuki syndrome and a literature review of 39 patients reported in ChinaHORMONE RESEARCH IN PAEDIATRICS, 2019, 91 : 443 - 443Chen, Ruimin论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R ChinaGong, Chunxiu论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Affiliated Beijing Children Hosp, Beijing, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R ChinaShangguan, Huakun论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R ChinaSu, Chang论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Affiliated Beijing Children Hosp, Beijing, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R ChinaOuyang, Qian论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R ChinaCao, Bingyan论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Affiliated Beijing Children Hosp, Beijing, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R ChinaWang, Jian论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Shanghai Childrens Med Cent, Shanghai, Peoples R China Fujian Med Univ, Teaching Hosp, Fuzhou Childrens Hosp Fujian Prov, Fuzhou, Fujian, Peoples R China
- [36] Identification of novel mutation in KMT2D gene in a patient with Kabuki syndrome and borderline chromosomal instabilityEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 992 - 993Pietrzyk, A.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Genet & Pathomorphol, Szczecin, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandLitwinska, Z.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Dept Gen Pathol, Szczecin, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandGos, M.论文数: 0 引用数: 0 h-index: 0机构: Inst Mother & Child Hlth, Dept Med Genet, Warsaw, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandBryskiewicz, M.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandStudniak, E.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandDlugoszewska, M.论文数: 0 引用数: 0 h-index: 0机构: Inst Mother & Child Hlth, Dept Med Genet, Warsaw, Poland Univ Warsaw, Fac Biol, Warsaw, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandGambin, T.论文数: 0 引用数: 0 h-index: 0机构: Inst Mother & Child Hlth, Dept Med Genet, Warsaw, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, PolandZajaczek, S.论文数: 0 引用数: 0 h-index: 0机构: Pomeranian Med Univ, Cytogenet Unit, Szczecin, Poland Pomeranian Med Univ, Dept Genet & Pathomorphol, Szczecin, Poland Pomeranian Med Univ, Cytogenet Unit, Szczecin, Poland
- [37] Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 geneANNALS OF NEUROLOGY, 2003, 54 (05) : 665 - 669Ugalde, C论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsTriepels, RH论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsCoenen, MJH论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, Netherlandsvan den Heuvel, LP论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsSmeets, R论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsUusimaa, J论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsBriones, P论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsCampistol, J论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsMajamaa, K论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsSmeitink, JAM论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, NetherlandsNijtmans, LGJ论文数: 0 引用数: 0 h-index: 0机构: Univ Nijmegen, Med Ctr, Dept Pediat, Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, Netherlands
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