Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Save this search Download search results Subscribe to news feed Your filters: cql: author="Balasubramanian, Meena" or (type any "bookEditor journalEditor issueEditor" and editor="B... Add to list Journal Article A1 ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder Stephanie Oates, Michael Absoud, Sushma Goyal, Sophie Bayley, Jennifer Baulcomb, Annemarie Sims, Amy Riddett, Katrina Allis, Charlotte Brasch-Andersen, Meena Balasubramanian, et al. (2021) CLINICAL GENETICS. 100(4). p.412-429 Add to list Journal Article A1 ZMYND11-related syndromic intellectual disability : 16 patients delineating and expanding the phenotypic spectrum Thabo M. Yates, Morgan Drucker, Angela Barnicoat, Karen Low, Erica H. Gerkes, Andrew E. Fry, Michael J. Parker, Mary O'Driscoll, Perrine Charles, Helen Cox, et al. (2020) HUMAN MUTATION. 41(5). p.1042-1050 Add to list Journal Article A1 Mutation update for the SATB2 gene Yuri A. Zarate, Katherine A. Bosanko, Aisling R. Caffrey, Jonathan A. Bernstein, Donna M. Martin, Marc S. Williams, Elizabeth M. Berry-Kravis, Paul R. Mark, Melanie A. Manning, Vikas Bhambhani, et al. (2019) HUMAN MUTATION. 40(8). p.1013-1029 Add to list Journal Article A1 open access Genotype-phenotype correlation in NF1 : evidence for a more severe phenotype associated with missense mutations affecting NF1 codons 844–848 Magdalena Koczkowska, Yunjia Chen, Tom Callens, Alicia Gomes, Angela Sharp, Sherrell Johnson, Meng-Chang Hsiao, Zhenbin Chen, Meena Balasubramanian, Christopher P Barnett, et al. (2018) AMERICAN JOURNAL OF HUMAN GENETICS. 102(1). p.69-87