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Number of items: 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-.


Aitken, Stuart, Firth, Helen V, McRae, Jeremy, Halachev, Mihail, Kini, Usha, Parker, Michael J, Lees, Melissa M, Lachlan, Katherine, Sarkar, Ajoy, Joss, Shelagh
et al (show 273 more authors) (2019) Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data. The American Journal of Human Genetics, 105 (5). pp. 933-946.


Ansari, Morad, Rainger, Jacqueline, Hanson, Isabel M, Williamson, Kathleen A, Sharkey, Freddie, Harewood, Louise, Sandilands, Angela, Clayton-Smith, Jill, Dollfus, Helene, Bitoun, Pierre
et al (show 43 more authors) (2016) Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. PLOS ONE, 11 (4). e0153757-.


Rainger, Joe, Keighren, Margaret, Keene, Douglas R, Charbonneau, Noe L, Rainger, Jacqueline K, Fisher, Malcolm, Mella, Sebastien, Huang, Jeffrey T-J, Rose, Lorraine, van't Hof, Rob
et al (show 3 more authors) (2013) A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse. PLOS GENETICS, 9 (12). e1003998-.

This list was generated on Wed Oct 4 04:53:44 2023 BST.