Molecular (FISH) and cytogenetic studies in the diagnosis of developmental delay in infants and children

Micronucleus assay as biomarker for chromosome malsegregation in young mothers with Down syndrome children

Chromosome 10 aneuploidy in pediatric acute lymphoblastic leukemia

Detection of 1(p36) deletion in patients with developmental delay and facial dysmorphism

Genetic study of neural tube defects

Karyotyping and neurodevelopmental follow-up ofintracytoplasmic sperm injection children up to4 years of age

Cytogenetics in acute leukemia and myelodysplastic syndrome

Detection of monosomy 7 in bone marrow failure pediatric patients

Cytogenic abnormalities of chromosome ARM 9P in leukemic patient

Genetic basis of developmental abnormalities of mid and hindbrain