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261by Zhuang-Zhuang Yuan, Zhuang-Zhuang Yuan, Zhuang-Zhuang Yuan, Liang-Liang Fan, Liang-Liang Fan, Zi-Chen Jiang, Yi-Feng Yang, Zhi-Ping Tan“... laterality defects, such as dextrocardia and heterotaxy syndrome. Laterality defects are a genetic condition...”
Published 2020-11-01
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262by Matthew Taylor, Dobromir Slavov, Ernesto Salcedo, Xiao Zhu, Deborah Ferguson, Jean Jirikowic, Andrea Di Lenarda, Gianfranco Sinagra, Luisa Mestroni“...Barth syndrome is an X-linked genetic condition featuring neutropenia, skeletal myopathy...”
Published 2011-07-01
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263by Michael P Schnetz, Lusy Handoko, Batool Akhtar-Zaidi, Cynthia F Bartels, C Filipe Pereira, Amanda G Fisher, David J Adams, Paul Flicek, Gregory E Crawford, Thomas Laframboise, Paul Tesar, Chia-Lin Wei, Peter C Scacheri“... syndrome, a genetic condition characterized by multiple congenital anomalies. To gain insights...”
Published 2010-07-01
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264by Linjun Chen, Lin Wang, Lei Chen, Fangyuan Wang, Fei Ji, Wei Sun, Hui Zhao, Weiju Han, Shiming Yang“...Background. Waardenburg syndrome is an uncommon genetic condition characterized by at least some...”
Published 2020-01-01
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265by Karolina Kobus, Daniela Hartl, Claus Eric Ott, Monika Osswald, Angela Huebner, Maja von der Hagen, Denise Emmerich, Jirko Kühnisch, Hans Morreau, Frederik J Hes, Victor F Mautner, Anja Harder, Sigrid Tinschert, Stefan Mundlos, Mateusz Kolanczyk“...<h4>Background</h4>Neurofibromatosis type I (NF1, MIM#162200) is a relatively frequent genetic...”
Published 2015-01-01
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266by Rayane Fraga, Pricila Sleifer, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen“... Introduction: Williams syndrome (WS) is a rare neurodevelopment genetic condition. The syndrome...”
Published 2019-07-01
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267by Aideen M. McInerney-Leo, Jennifer West, Bettina Meiser, Malcolm West, Matthew A. Brown, Matthew A. Brown, Emma Duncan, Emma Duncan“... MFS was a genetic condition, many speculated about the role of non-genetic causes in initiating...”
Published 2020-05-01
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268by Vandana Jain, Santosh Kumar, Naval K Vikram, Mani Kalaivani, Surya Prakash Bhatt, Rajni Sharma, Kumar Kabra Sushil“...Background & objectives: Cystic fibrosis (CF) is a life-limiting genetic condition resulting...”
Published 2017-01-01
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269“... disorders or any other genetic condition. Microarrays are one of the main high-throughput technologies...”
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270by Patrick M. Cowley, Divya R. Nair, Lara R. DeRuisseau, Stefan Keslacy, Mustafa Atalay, Keith C. DeRuisseau“...Down syndrome (DS) is a genetic condition caused by the triplication of chromosome 21. Persons...”
Published 2017-10-01
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271by Sónia Ferreira, Andreia Carvalho Pereira, Bruno Quendera, Aldina Reis, Eduardo Duarte Silva, Miguel Castelo-Branco“... Pigmentosa (RP), a genetic condition leading to peripheral visual degeneration. We acquired functional...”
Published 2017-01-01
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272by Joanna Kohut, Bogusław Mazurek, Jacek Pająk, Lesław Szydłowski, Aleksandra Morka“...Tuberous sclerosis complex is a genetic condition with an autosomal dominant pattern of inheritance...”
Published 2017-06-01
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273“... occulta and tarsal coalitions), were the result of a genetic condition. The isotopic analysis shows...”
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274“... micronuclei(MN) frequency has been associated with various exposure and genetic condition. Recent studies show...”
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275by Moller, Hendrina Cecilia“... as a neuro-genetic condition and the manner whereby it manifests itself in various learning...”
Published 2015
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276by Mazar, Iyar“..., genetic condition in males associated with life-limiting and life-threatening symptoms. Research...”
Published 2019
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277by Enzo R Porrello, Catherine E Huggins, Claire L Curl, Andrea A Domenighetti, Thierry Pedrazzini, Leanne MD Delbridge, Trefor O Morgan“... pre-existing genetic condition of Ang II-dependent cardiac hypertrophy, the pro-growth effect...”
Published 2004-12-01
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278by Iris D. Noordman, Janiëlle AEM. van der Velden, Henri JLM. Timmers, Nicole Reisch, Annette Richter-Unruh, Catherine Pienkowksi, Nel Roeleveld, Hedi L. Claahsen-van der Grinten“...Background: Turner syndrome (TS) is a genetic condition with a broad phenotypic spectrum...”
Published 2021-02-01
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279by Blake, Yvonne“... on its function in dreaming exists. Urbach-Wiethe Disease (UWD) is a very rare genetic condition that can...”
Published 2015
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Dissertation -
280by Małgorzata Kałużna, Pola Kompf, Michał Rabijewski, Jerzy Moczko, Jarosław Kałużny, Katarzyna Ziemnicka, Marek Ruchała“...(1) Background: Isolated hypogonadotropic hypogonadism (IHH) is a genetic condition characterized...”
Published 2021-06-01
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