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Leukemia & Lymphoma|December 30, 2020
The propriety of upgrading responses to venetoclax + azacitidine in newly diagnosed patients with acute myeloid leukemiaDiana Abbott, Evan Cherry, Maria Amaya, et al.Clinical Dysmorphology|December 12, 2022
3MC syndrome: molecular findings in previously reported and milder patients expand the natural history and phenotypic spectrumChloe Jade Ashton, Rahat Perveen, Glenda Beaman, et al.Human Genetics|October 18, 2002
Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene regionDavid Monk, Louise Bentley, Megan Hitchins, et al.Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.European Journal of Medical Genetics|October 24, 2006
Tall stature and duplication of the insulin-like growth factor I receptor geneS G Kant, M Kriek, M J E Walenkamp, et al.Journal of Medical Case Reports|November 21, 2008
Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case reportGregory J Fitzgibbon, Jill Clayton-Smith, Siddharth Banka, et al.The Cochrane Database of Systematic Reviews|November 8, 2016
Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the childJennifer Weston, Rebecca Bromley, Cerian F Jackson, et al.Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.Investigative Ophthalmology & Visual Science|January 10, 2015
Abrogation of HMX1 function causes rare oculoauricular syndrome associated with congenital cataract, anterior segment dysgenesis, and retinal dystrophyRachel L Gillespie, Jill Urquhart, Simon C Lovell, et al.Journal of Medical Genetics|June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndromeS Lindsay, M Ireland, O O'Brien, et al.Pageof 36