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201by Shivcharan L Chandravanshi, Ashok Kumar Rawat, Prem Chand Dwivedi, Pankaj Choudhary“...The Hutchinson-Gilford progeria (HGP) syndrome is an extremely rare genetic condition characterized...”
Published 2011-01-01
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202“...Fibrodysplasia ossificans progressiva (FOP) is a rare genetic condition characterized...”
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203by Farmaditya E. P. Mundhofir, Helger G. Yntema, Ineke van der Burgt, Ben C. J. Hamel, Sultana M. H. Faradz, Bregje W. M. van Bon“...Mowat-Wilson syndrome (OMIM 235730) is a genetic condition characterized by moderate-to-severe...”
Published 2012-01-01
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204by Albrecht, Sara Kathryn“..., the researcher studied individuals with Williams syndrome (WS), a genetic condition which has the hallmark...”
Published 2009
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205“... for identifying people at risk for a genetic condition by a process of systematic family tracing....”
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206“... for patient’s dental health. Progeria is a rare genetic condition where symptoms resembling aspects of aging...”
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207“..., BrazilAbstract: Prader–Willi syndrome is a rare genetic condition afflicting nearly 1/15,000 live births...”
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208by Yifeng Ding, Ji Wang, Shuizhen Zhou, Yuanfeng Zhou, Linmei Zhang, Lifei Yu, Yi Wang“...Tuberous sclerosis complex (TSC) is a genetic condition characterized by the occurrence...”
Published 2020-03-01
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209by Camille de Seynes, C. Ged, H. de Verneuil, N. Chollet, M. Balduyck, C. Raherison“...Alpha-1-antitrypsin deficiency (A1ATD) is a genetic condition caused by SERPINA1 mutations, which...”
Published 2017-01-01
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210by Malgorzata I Wiweger, Zhe Zhao, Richard J P van Merkesteyn, Henry H Roehl, Pancras C W Hogendoorn“... dominant genetic condition that is characterized by the formation of cartilaginous bone tumours...”
Published 2012-01-01
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211by Miguel Augusto Martins Pereira, Lygia Marina Mendes da Costa, Suelen Brito Nascimento, Hye Chung Kang, Adelmo Henrique Daumas Gabriel“... into primary and secondary (or reactive), the first, also known as familial HLH, is a genetic condition...”
Published 2021-11-01
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212by Harith, N. S. B.“... genetic condition, where mutations of COL1A1 and COL1A2 genes result in variations of the collagen α...”
Published 2013
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213by Bailey, Pippa“... with cerebral palsy, one with autistic spectrum disorder and one with a genetic condition. Data collection took...”
Published 2013
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214by Weeple, Paula K.“... secondary to cystic fibrosis, a pre-existing, life threatening, genetic condition. The purpose of this study...”
Published 2004
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215by Tahaei, Seyedmohammad Ebrahim“.... This common genetic condition is associated with tibial pseudarthrosis (PA), whose etiology is unknown...”
Published 2018
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216by Nesbitt, Victoria“... impairment is an early feature, although may not be recognized as part of an underlying genetic condition...”
Published 2015
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217by Harlalka, Gaurav Vijay“..., leading to a significant reduction in HERC2 levels in affected individuals. e The third genetic condition...”
Published 2015
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218by Gavlak, J. C. D.“...) is the most common genetic condition in the UK. A high prevalence of Sleep Disordered Breathing (SDB) in SCA...”
Published 2016
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219“...Abstract Background Huntington's disease (HD) is a genetic condition resulting in movement...”
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220by Castro, Aimee R, Chougui, Khadidja, Bilodeau, Claudette, Tsimicalis, Argerie“... BackgroundOsteogenesis imperfecta (OI) is a rare genetic condition that can...”
Published 2019-12-01
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