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Stem Cell Research|May 16, 2025
Two iPSC lines with a heterozygous frameshift mutation in the floating-harbour syndrome locus of the SRCAP geneJ Rhode, S Edwards, A Tzvetkova, et al.Stem Cell Research|March 31, 2024
Generation of two isogenic iPSC lines from a healthy male donor of European ancestryS Edwards, L Hagenau, B Nowack, et al.American Journal of Human Genetics|March 31, 2000
Similar splice-site mutations of the ATP7A gene lead to different phenotypes: classical Menkes disease or occipital horn syndromeL B Møller, Z Tümer, C Lund, et al.Cytogenetic and Genome Research|January 21, 2012
A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate corticesE Schneider, L R Jensen, R Farcas, et al.Journal of the American College of Cardiology|December 1, 1996
Relation between gender, etiology and survival in patients with symptomatic heart failureK F Adams, S H Dunlap, C A Sueta, et al.Cytogenetic and Genome Research|March 30, 2012
Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate corticesE Schneider, S Mayer, N El Hajj, et al.Journal of Medical Genetics|September 20, 2005
Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGHD Lugtenberg, A P M de Brouwer, T Kleefstra, et al.Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.Pageof 2