MACRODONTIA: A brief overview and a case report of KBG syndrome by Manogari Chetty, BChD, BSc, MChD, PhD, Khaled Beshtawi, BDS, MSc, Imaan Roomaney, BChD, MPH, Salma Kabbashi, BDS, MSc

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Anesthetic Management of Children with KBG Syndrome and Novel Use of Sacral Erector Spinae Block: A Case Report by Sana Y. Hussain, Nishant Patel, Anju Gupta, Nupur Pandya

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A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and review of the literature by Tianqin Deng, Qingzhi Liu, Jiansheng Xie, Xuemei Li, Bing Yao

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A case report of a preterm infant with KBG syndrome and hepatoblastoma by Kyoung Sung Yun, Seung Han Shin, Jaemoon Koh, Jung Min Ko, Jung Yoon Choi, Nam-Joon Yi

Subjects: “…KBG syndrome…”
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Epileptic dyskinetic encephalopathy in KBG syndrome: Expansion of the phenotype by Eoin P. Donnellan, Kathleen M. Gorman, Amre Shahwan, Nicholas M. Allen

Subjects: “…KBG syndrome…”
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KBG syndrome by Dayna Morel Swols, Joseph Foster, Mustafa Tekin

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Identification of a novel frameshift variation in ANKRD11: a case report of KBG syndrome by Qing Shao, Qiang Jiang, Yuqi Luo, Yimei Meng, Guoyu Tian, Xiao Yin

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Neurobehavioral characteristics of mice with SETD5 mutations as models of IDD23 and KBG syndromes by Tadashi Nakagawa, Tadashi Nakagawa, Satoko Hattori, Toru Hosoi, Keiko Nakayama

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Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review by Su Jin Kim, Aram Yang, Ji Sun Park, Dae Gyu Kwon, Jeong-Seop Lee, Young Se Kwon, Ji Eun Lee

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KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature by Yunha Choi, Jungmin Choi, Hyosang Do, Soojin Hwang, Go Hun Seo, In Hee Choi, Changwon Keum, Jin‐Ho Choi, Minji Kang, Gu‐Hwan Kim, Han‐Wook Yoo, Beom Hee Lee

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SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome by Milena Crippa, Milena Crippa, Ilaria Bestetti, Ilaria Bestetti, Silvia Maitz, Karin Weiss, Alice Spano, Maura Masciadri, Sarah Smithson, Lidia Larizza, Karen Low, Lior Cohen, Lior Cohen, Palma Finelli, Palma Finelli

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The Chromatin Regulator Ankrd11 Controls Palate and Cranial Bone Development by Daniela Marta Roth, Pranidhi Baddam, Haiming Lin, Marta Vidal-García, Jose David Aponte, Sarah-Thea De Souza, Devyn Godziuk, Adrianne Eve Scovil Watson, Tim Footz, Nathan F. Schachter, Nathan F. Schachter, Sean E. Egan, Sean E. Egan, Benedikt Hallgrímsson, Daniel Graf, Daniel Graf, Anastassia Voronova, Anastassia Voronova

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Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndrome by Shuoshuo Wei, Yanying Li, Wanling Yang, Shuxiong Chen, Fupeng Liu, Mei Zhang, Bo Ban, Dongye He

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Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search by Dongye He, Mei Zhang, Yanying Li, Fupeng Liu, Bo Ban

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Case Report: Two Newly Diagnosed Patients With KBG Syndrome—Two Different Molecular Changes by Katarzyna Wojciechowska, Joanna Nurzyńska-Flak, Borys Styka, Magdalena Kacprzak, Monika Lejman

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