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Pratt, Harry, Williams, Bryan M ORCID: 0000-0001-5930-287X, Ku, Jae Yee, Vas, Charles, McCann, Emma, Al-Bander, Baidaa, Zhao, Yitian, Coenen, Frans ORCID: 0000-0003-1026-6649 and Zheng, Yalin ORCID: 0000-0002-7873-0922
(2018) Automatic Detection and Distinction of Retinal Vessel Bifurcations and Crossings in Colour Fundus Photography. JOURNAL OF IMAGING, 4 (1). p. 4.


Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H, Nowak, Catherine B, Douglas, Jessica, Swoboda, Kathryn J
et al (show 368 more authors) (2019) CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018). NATURE COMMUNICATIONS, 10 (1). 883-.


Mithyantha, Renuka, Kneen, Rachel, McCann, Emma and Gladstone, Melissa ORCID: 0000-0002-2579-9301
(2017) Current evidence-based recommendations on investigating children with global developmental delay. ARCHIVES OF DISEASE IN CHILDHOOD, 102 (11). pp. 1071-1076.

This list was generated on Sat Jan 6 21:55:52 2024 GMT.