… (31), and 391 (88%) are within 5 kb of known human islet active chromatin DNase, FAIRE, or
… this new gene locus is in a ∼10-kb region nominally significant in the MAGIC database for …

Background: Patients with facioscapulohumeral muscular dystrophy (FSHD) show a contraction
of the D4Z4 repeat array in the subtelomere of chromosome 4q. This D4Z4 contraction is …

Bannayan–Riley–Ruvalcaba syndrome (BRRS) is characterised by macrocephaly, intestinal
hamartomatous polyps, lipomas, pigmented maculae of the glans penis, developmental …

Submicroscopic deletion of the terminal part of the short arm of chromosome 6, including
6p25, leads to developmental retardation, hearing impairment, ocular dysgenesis, and …

High-resolution analyses of complex chromosome rearrangements (CCR) have demonstrated
in individuals with abnormal phenotypes that not all seemingly balanced CCRs based on …

A comment on this article appears in"[Risk factors for structural chromosomal abnormality in>
or= 2 miscarriages, as an instrument for selective karyotyping]." Ned Tijdschr Geneeskd. …

Copy number variations (CNVs) on the short arm of chromosome 19 are relatively rare. We
present a patient with a tandem de novo 3.9 Mb duplication of 19p13.12p13.2 and an …

A major challenge in understanding differences in electric propulsion performance in ground
tests and in space operations concerns the pressure distribution within the test vacuum …

… To identify early glial precursors, we created GFAPpromoter-lacZ transgenic mice, using a
1.8kb 5′ fragment of human GFAP. The expression of the transgene was first detected in the …

… (2.2 kb) were also found in the developing rat testis after 30 … the RI0 (1.7 kb) and RIIa (2.2
kb) mRNA on the age studies … , 2.9 kb) mRNA bands, but not to the small-sized mRNA (1.7 kb). …