Latest papers

Mosaic ring chromosome 8: clinical and array-CGH findings in partial trisomy 8.

Complex and segmental uniparental disomy updated.

Clinical course of a 20-month-old child diagnosed prenatally with mosaic ring chromosome 18 and monosomy 18.

Evolutionary and clinical neocentromeres: two faces of the same coin?

Ring chromosome 12 and severe oligospermia: a case report.

Intracytoplasmic sperm injection (ICSI) with transmission of a ring(Y) chromosome and ovotesticular disorder of sex development in offspring.

Kidney abnormalities in persons with monosomy 15q26.

Two circular chromosomes of unequal copy number make up the mitochondrial genome of the rotifer Brachionus plicatilis.

Adult transitional pre-B acute lymphoblastic leukemia associated with ring chromosome 16.

An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.

High-resolution array CGH analysis of salivary gland tumors reveals fusion and amplification of the FGFR1 and PLAG1 genes in ring chromosomes.

Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman.

Ring chromosome 7 in an Indian woman.

Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia.

Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.

Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicism.

Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism.

[Gytogenetics of Chironomus riparius L. from the fishpond in Borok village (Diptera, Chironomidae)].

Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia.

Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12.