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241by Amira A Abdelazeem, Olfat A Hassanin, Amal A Elgohary, Maha S Zaki, Amany H Galal, Joseph G Gleeson“... and by prior publications should be evaluated as potentially independent of the primary genetic condition...”
Published 2017-01-01
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Article -
242by Pachet Corinne, Barreau Lise, Frebourg Thierry, Caron Olivier, Rahal Arslane, Delaloge Suzette, Heymann Steve, Mathieu Marie-Christine, Marsiglia Hugo, Bourgier Céline“... of breast cancer patients with germ-line p53 mutations, an exceptional genetic condition, particularly...”
Published 2010-11-01
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243by Ikuo Watanobe, Hiroko Kida, Yuuki Sekine, Masaya Kawai, Shozo Miyano, Michio Machida, Toshiaki Kitabatake, Hiroyuki Sugo, Yoshifumi Lee, Kuniaki Kojima“...Congenital epidermolysis bullosa is a rare, genetic condition in which even slight stimulation can...”
Published 2018-01-01
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244by Matías-Pérez D, Pérez-Santiago AD, Sánchez Medina MA, Alpuche Osorno JJ, García-Montalvo IA“... genetic condition, the secondary expression of a primary process or the consequence of exogenous factors...”
Published 2021-07-01
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245by Moller, Hendrina Cecilia“... as a neuro-genetic condition and the manner whereby it manifests itself in various learning...”
Published 2015
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246by Pithara, Christalla“.... patient experience, were found to be influenced by factors associated with the genetic condition...”
Published 2011
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247by Hall, Jessica H.“...Down’s syndrome is a complex genetic condition arising from trisomy of chromosome 21...”
Published 2016
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248by Taifeng Zhou, Yongqian Wang, Hang Zhou, Zhiheng Liao, Bo Gao, Deying Su, Shuhui Zheng, Caixia Xu, Peiqiang Su“...Abstract Background Multiple epiphyseal dysplasia (MED) is a heterogeneous genetic condition...”
Published 2018-05-01
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249by Paula Tanabe, Audrey L. Blewer, Emily Bonnabeau, Hayden B. Bosworth, Denise H. Clayton, Nancy Crego, Marian F. Earls, Kern Eason, Grayson Forlines, Gary Rains, Matthew Young, Nirmish Shah“...**Background:** Sickle cell disease (SCD) is a genetic condition affecting primarily individuals...”
Published 2021-04-01
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250by Goliath, Rene“.... The main broad themes include "a roller coaster journey," "learning how to survive," "a genetic condition...”
Published 2018
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Dissertation -
251by Daniele De Brasi, Francesca Orlando, Valeria Gaeta, Maria De Liso, Fabio Acquaviva, Luigi Martemucci, Augusto Mastrominico, Maja Di Rocco“...Fibrodysplasia ossificans progressiva (FOP) is an ultrarare genetic condition characterized...”
Published 2021-07-01
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252by Mathew N. Leslie, Joshua Chou, Paul M. Young, Daniela Traini, Peta Bradbury, Hui Xin Ong“... to a genetic condition (Alpha-1 antitrypsin deficiency) or exposure to pollutants/irritants...”
Published 2021-08-01
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253“...: genetic condition, treatment method, blood markers, nutritional status, daily living, state of health...”
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254“... and treating gingival enlargements. If a genetic condition is suspected, genetic screening is also needed. All...”
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255“.... Patients with G6PD deficiency, an X-linked recessive genetic condition, can not contact or take camphor...”
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256by Berendt Agnieszka, Wójtowicz-Marzec Monika, Wysokińska Barbara, Kwaśniewska Anna“...Abstract Background Haemophilia A is an X-linked genetic condition which manifests itself mainly...”
Published 2021-07-01
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257by Gioia Mastromoro, Giulio Calcagni, Paolo Versacci, Carolina Putotto, Marcello Chinali, Caterina Lambiase, Marta Unolt, Elena Pelliccione, Silvia Anaclerio, Cinzia Caprio, Sara Cioffi, Marchesa Bilio, Anwar Baban, Fabrizio Drago, Maria Cristina Digilio, Bruno Marino, Antonio Baldini“... tract and great arteries. However, in this genetic condition the dimensions of the pulmonary arteries...”
Published 2019-01-01
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258by D. Hettiarachchi, Hetalkumar Panchal, B. A. P. S. Pathirana, P. D. Rathnayaka, A. Padeniya, P. S. Lai, V. H. W. Dissanayake“...Introduction. Ataxia telangiectasia is a rare genetic condition with an estimated prevalence of 1...”
Published 2020-01-01
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259by Gara Samara Brajadenta, Ariestya Indah Permata Sari, Donny Nauphar, Tiar Masykuroh Pratamawati, Vincent Thoreau“... genetic condition, with autosomal dominant inheritance, characterized by craniosynostosis, midfacial...”
Published 2019-08-01
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260“... to seizures as well, as 30% of patients with oculodentodigital dysplasia (ODDD), a rare genetic condition...”
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Article