Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22

CYTOGENETIC STUDY OF CHILDREN WITH DEVELOPMENTAL DELAY AND ASSOCIATED ANOMALIES

Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion

Females with Gonadal Dysgenesis: Cytogenetic and Molecular Analysis

Non- Disjunction of Chromosome 21 in the Young Mother at Conception

Cytogenetic study of a large cohort of patients with corpus callosum abnormalities

Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation

Cytogenetic Study in Couples with Recurrent Miscarriage

Copy number variants in chromosomes 15& 16 and its contribution to phenotypic aspects in autistic children

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