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Article

Blok, LS, Rousseau, J, Twist, J et al. (376 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. 883. ISSN 2041-1723

Bengani, H, Handley, M orcid.org/0000-0001-7200-747X, Alvi, M et al. (31 more authors) (2017) Clinical and molecular consequences of disease-associated de novo mutations in SATB2. Genetics in Medicine, 19 (8). pp. 900-908. ISSN 1098-3600

McRae, JF, Clayton, S, Fitzgerald, TW et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542. pp. 433-438. ISSN 0028-0836

Kang, YJ, Lees, M, Matthews, LC et al. (3 more authors) (2015) miR-145 suppresses embryo-epithelial juxtacrine communication at implantation by modulating maternal IGF1R. Journal of Cell Science, 128 (4). pp. 804-814. ISSN 0021-9533

Forbes, K, Lees, M, Kang, Y-J et al. (2 more authors) (2014) O-079 Regulation of Implantation by Interaction between the Type-1 IGF Receptor (IGF1R) and MiR-145. Reproductive Sciences, 21 (3). 102A-102A. ISSN 1933-7191

This list was generated on Sun Sep 22 08:22:46 2019 BST.