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