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Number of items: 5.

Balasubramanian, Meena, Dingemans, Alexander J. M., Albaba, Shadi, Richardson, Ruth, Yates, Thabo M., Cox, Helen, Douzgou, Sofia, Armstrong, Ruth, Sansbury, Francis H., Burke, Katherine B., Fry, Andrew E., Ragge, Nicola, Sharif, Saba, Foster, Alison, De Sandre-Giovannoli, Annachiara, Elouej, Sahar, Vasudevan, Pradeep, Mansour, Sahar, Wilson, Kate, Stewart, Helen, Heide, Solveig, Nava, Caroline, Keren, Boris, Demirdas, Serwet, Brooks, Alice S., Vincent, Marie, Isidor, Bertrand, Küry, Sebastien, Schouten, Meyke, Leenders, Erika, Chung, Wendy K., Haeringen, Arie van, Scheffner, Thomas, Debray, Francois-Guillaume, White, Susan M., Palafoll, Maria Irene Valenzuela, Pfundt, Rolph, Newbury-Ecob, Ruth and Kleefstra, Tjitske 2021. Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. European Journal of Human Genetics 10.1038/s41431-020-00769-7
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Burke, Katherine Bernadette 2018. Array comparative genomic hybridisation and the newborn intensive care unit: Sociological perspectives on mainstreaming medical genetics. PhD Thesis, Cardiff University.
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Burke, Katherine, Howard, Zoe and Kamath, Arveen 2017. Genetic and genomic investigations in the neonatal intensive care unit. Paediatrics and Child Health 27 (1) , pp. 23-27. 10.1016/j.paed.2016.08.001

Burke, Katherine and Clarke, Angus 2016. The challenge of consent in clinical genome-wide testing. Archives of Disease in Childhood 101 , pp. 1048-1052. 10.1136/archdischild-2013-304109

Burke, Katherine and Clarke, Angus 2015. Genetic screening. In: Henk, ten Have, ed. Encyclopedia of Global Bioethics, Springer Reference,

This list was generated on Sat Feb 27 04:17:35 2021 GMT.