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Alcoholism, Clinical and Experimental Research|September 30, 2021
Prevalence of fetal alcohol spectrum disorder in Greater Manchester, UK: An active case ascertainment studyRobyn McCarthy, Raja A S Mukherjee, Kate M Fleming, et al.
American Journal of Medical Genetics. Part A|March 21, 2019
Genotype-phenotype specificity in Menke-Hennekam syndrome caused by missense variants in exon 30 or 31 of CREBBPSiddharth Banka, Rebecca Sayer, Catherine Breen, et al.
Experimental Hematology|May 29, 2019
CD123 CAR T cells for the treatment of myelodysplastic syndromeBrett M Stevens, Wei Zhang, Daniel A Pollyea, et al.
European Journal of Medical Genetics|May 4, 2019
Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanismsA Redwood, S Douzgou, S Waller, et al.
Cancer Research|August 28, 2003
Histone deacetylase inhibitor LAQ824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cellsRamadevi Nimmanapalli, Lianne Fuino, Purva Bali, et al.
Genome Research|December 21, 2013
A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disordersDaniel A King, Tomas W Fitzgerald, Ray Miller, et al.
American Journal of Medical Genetics. Part A|July 9, 2011
Five patients with novel overlapping interstitial deletions in 8q22.2q22.3Alma Kuechler, Karen Buysse, Jill Clayton-Smith, et al.
Epilepsia|July 17, 2010
Early cognitive development in children born to women with epilepsy: a prospective reportRebecca L Bromley, George Mawer, Jenna Love, et al.
European Journal of Medical Genetics|March 21, 2007
A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25-q26Deirdre D Cilliers, Rahat Parveen, Peter Clayton, et al.
Eye (London, England)|June 18, 2016
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approachM Musleh, G Hall, I C Lloyd, et al.
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