Latest papers

Fetal facial profile in Pallister-Killian syndrome.

Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.

[A case of acute promyelocytic leukemia with double ider (17q-)].

An extranodal nasal natural killer/T-cell lymphoma with isochromosome 7q10 as the sole cytogenetic aberration was initially diagnosed via bone marrow biopsy.

Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns.

Concomitant appearance of trisomy 8 and isochromosome 17q in a Philadelphia-positive clone in a patient with chronic myeloid leukemia in chronic phase: an alarm for changing therapeutic strategy.

A case of Pallister-Killian syndrome associated with West syndrome.

[Mixed gonadal dysgenesis associated with an isodicentric Y chromosome].

[Exacerbation of acute leukemia bearing isolated i(17q) along with proliferation of blasts with high BMI-1 expression].

Delineation of an isodicentric Y chromosome in a mosaic 45,X/46,X,idic(Y)(qter-p11.3::p11.3-qter) fetus by SRY sequencing, G-banding, FISH, SKY and study of distribution in different tissues.

Two cases of isochromosome 18q syndrome.

Monitoring the isochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR.

Pregnancy and postnatal outcome of mosaic isochromosome 20q.

Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male.

Imaging of silkworm meiotic chromosome by atomic force microscopy.

High cognitive functioning and behavioral phenotype in Pallister-Killian syndrome.

Phenotypic variability in isodicentric Y patients: study of nine cases.

Aneuploidy and isochromosome formation in drug-resistant Candida albicans.

Characterization of a maize isochromosome 8S*8S.

Isochromosome 1q in a myelodysplastic syndrome after treatment for acute promyelocytic leukemia.