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

The implication of (FISH) technique indetection of chromosomal anomalies

Chromosomal study in microcephly

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

Detection of monosomy 7 in bone marrow failure pediatric patients

Cytogenetics in acute leukemia and myelodysplastic syndrome

Molecular genetics of childhood acutelymphoblastic leukemia and implications forprognosis and treatment

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

Chromosome 10 aneuploidy in pediatric acute lymphoblastic leukemia

Study of TEL-AML1 fusion gene in B-lineage acute lymphoblastic leukemia using fish