Prenatal diagnosis of 9q34.3 microdeletion-associated Kleefstra syndrome in a pregnancy complicated by polyhydramnios: A case report and literature review by Yi-Yun Tai, Chih-Ling Chen, Chen-Tu Wu, Chien-Nan Lee, Shin-Yu Lin

Subjects: “…Kleefstra syndrome…”
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Kleefstra Syndrome: The First Case Report From Iran by Mehrdad Noruzinia, Mohammad Ahmadvand, Oranous Bashti, Ahmad Reza Salehi Chaleshtori

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A Korean male with Kleefstra syndrome presented with micropenis by Rosie Lee, Mi-seon Lee, Jung Eun Moon

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Presentation of Kleefstra syndrome; case report by Javad Akhondian, Neda Fakhr Ghasemi

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Presentation of Kleefstra syndrome; case report by Javad Akhondian, Neda Fakhr Ghasemi

Subjects: “…kleefstra syndrome ehmt1 gene neurodevelopmental delay…”
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De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome 2: Case Report and Literature Review by Maria Anna Siano, Ilaria De Maggio, Roberta Petillo, Dario Cocciadiferro, Emanuele Agolini, Massimo Majolo, Antonio Novelli, Matteo Della Monica, Carmelo Piscopo

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Clinical characteristics and genetic analysis of four pediatric patients with Kleefstra syndrome by Rong Ren, Yedan Liu, Peipei Liu, Jing Zhao, Mei Hou, Shuo Li, Zongbo Chen, Aiyun Yuan

Subjects: “…Kleefstra syndrome-1 (KLEFS1)…”
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Kleefstra syndrome combined with vesicoureteral reflux and rectourethral fistula: a case report and literature review by Chae Won Lee, Min Ji Park, Eun Joo Lee, Sangyoon Lee, Jinyoung Park, Jun Nyung Lee, So Mi Lee, Shin Young Jeong, Min Hyun Cho

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Case Report: Long-Term Treatment and Follow-Up of Kleefstra Syndrome-2 by Dandan Wu, Rong Li

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Kleefstra syndrome and epilepsy by R. G. Gamirova, N. G. Lyukshina, R. R. Gamirova, M. E. Farnosova

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Psychiatric manifestations of Kleefstra syndrome: a case report by Kazunari Yoshida, Kazunari Yoshida, Kazunari Yoshida, Daniel J. Müller, Daniel J. Müller, Daniel J. Müller, Daniel J. Müller, Pushpal Desarkar, Pushpal Desarkar, Pushpal Desarkar, Pushpal Desarkar

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A multi-layered computational structural genomics approach enhances domain-specific interpretation of Kleefstra syndrome variants in EHMT1 by Young-In Chi, Salomão D. Jorge, Davin R. Jensen, Brian C. Smith, Brian F. Volkman, Angela J. Mathison, Gwen Lomberk, Michael T. Zimmermann, Raul Urrutia

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Establishment of human pluripotent stem cell-derived cortical neurosphere model to study pathomechanisms and chemical toxicity in Kleefstra syndrome by Andrea Balogh, Mária Bódi-Jakus, Vivien Réka Karl, Tamás Bellák, Balázs Széky, János Farkas, Federica Lamberto, David Novak, Anita Fehér, Melinda Zana, András Dinnyés

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Tourette-like syndrome secondary to Kleefstra syndrome 1 with a de novo microdeletion in the EHMT1 gene by Mengyue Niu, Yanjing Li, Shikun Zhan, Bomin Sun, Jun Liu, Yiwen Wu

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EHMT1 mosaicism in apparently unaffected parents is associated with autism spectrum disorder and neurocognitive dysfunction by Anneke de Boer, Karlijn Vermeulen, Jos I. M. Egger, Joost G. E. Janzing, Nicole de Leeuw, Hermine E. Veenstra-Knol, Nicolette S. den Hollander, Hans van Bokhoven, Wouter Staal, Tjitske Kleefstra

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Anesthesia and pain management of a patient with Kleefstra Syndrome for robotic ureteral reimplantation. by E. D. Van Der Zwaag, N. A. Bohannon, S. L. Thompson, J. K. Goeller

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Genotype-phenotype correlations in a fetus with Kleefstra syndrome by Xuezhen Wang, Jiebin Wu, Min Pang, Ying Liu, Jingfang Zhai

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Novel germline variants in KMT2C in Chinese patients with Kleefstra syndrome-2 by Qi Yang, Qi Yang, Qiang Zhang, Qiang Zhang, Sheng Yi, Sheng Yi, Shujie Zhang, Shujie Zhang, Shang Yi, Shang Yi, Xunzhao Zhou, Xunzhao Zhou, Zailong Qin, Zailong Qin, Biyan Chen, Biyan Chen, Jingsi Luo, Jingsi Luo, Jingsi Luo

Subjects: “…Kleefstra syndrome-2…”
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