Disease: Recombinant chromosome 8 syndrome
- A 590 kb deletion caused by non-allelic homologous recombination between two LINE-1 elements in a patient with mesomelia-synostosis syndrome
- Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of "8p Inverted Duplication/Deletion Syndrome"
- Clinical phenotype and genetic analysis of a fetus with recombinant chromosome 8 syndrome
- Clinicopathologic and dysmorphic findings in recombinant chromosome 8 syndrome
- De Novo San Luis Valley Syndrome-like der(8) Chromosome With a Concomitant dup(8p22) in a Mexican Girl
- Generation of induced pluripotent stem cell GZHMCi005-A from amniotic fluid-derived cells with duplication of chromosome 8p
- Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses
- Mapping of new quantitative trait loci for sudden death syndrome and soybean cyst nematode resistance in two soybean populations
- Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowth
- Myeloproliferative neoplasms with t(8;22)(p11.2;q11.2)/BCR-FGFR1: a meta-analysis of 20 cases shows cytogenetic progression with B-lymphoid blast phase
- Neuroimaging Features of San Luis Valley Syndrome
- Postnatal diagnosis of de novo complex der(8) in a boy with prenatal diagnosis of recombinant chromosome 8 syndrome
- Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity
- Pre- and postnatal findings in a patient with a novel rec(8)dup(8q)inv(8)(p23.2q22.3) associated with San Luis Valley syndrome
- Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature
- PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome
- Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks
- Revisiting recombinant 8 syndrome