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CytogeneticsFollow by RSS 

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keywords > Natural Science Disciplines > Biological Science Disciplines > Biology > Genetics > Cytogenetics

Latest papers

Rubinstein-Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: a contiguous gene syndrome?

Molecular cytogenetic characterization of a new case of partial trisomy 13 (13q11q13.2).

Prenatal study of common submicroscopic genomic disorders using MLPA with subtelomeric/microdeletion syndrome probe mixes, among gestations with ultrasound abnormalities in the first trimester.

Characterization of a de novo balanced translocation t(9;18)(p23;q12.2) in a patient with oculoauriculovertebral spectrum

Occurrence of natural triploidy in Rhamdia quelen (Siluriformes, Heptapteridae).

[Liver cirrhosis patogenetics: polymorphism of glutation S-transferase genes].

Cytogenetic evidence for de novo synthesis of rRNA and involvement of nucleolar material in the organization of cell structures during spermiogenesis of Chariesterus armatus (Heteroptera, Coreidae).

Molecular pathology and patient care.

Cytogenetic and molecular characterization of plutonium-induced rat osteosarcomas.

[Hryhoriĭ Andriĭovych Levyts'kyĭ--Ukrainian cytogeneticist and karyotyping specialist (1878-1943)].

Retinal mass in a case of pediatric myelodysplastic syndrome (refractory anemia with excess of blasts).

Performance of human immunostimulating agents in the improvement of fish cytogenetic preparations.

Prenatal study of common submicroscopic “genomic disorders” using MLPA with subtelomeric/microdeletion syndrome probe mixes, among gestations with ultrasound abnormalities in the first trimester

Efficacy of lenalidomide in patients with chronic lymphocytic leukemia with high-risk cytogenetics.

ZAP-70, IgVh, and cytogenetics for assessing prognosis in chronic lymphocytic leukemia.

Genetic changes including gene copy number alterations and their relation to prognosis in childhood acute myeloid leukemia.

A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

Frequent CD7 antigen loss in aggressive natural killer-cell leukemia: a useful diagnostic marker.

Pharmacogenetics: technologies to detect copy number variations.

Correlation of flow cytometrically determined expression of ZAP-70 using the SBZAP antibody with IgVH mutation status and cytogenetics in 1,229 patients with chronic lymphocytic leukemia.

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