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Indian Pediatr ; 2008 Jul; 45(7): 595-8
Article in English | IMSEAR | ID: sea-12262

ABSTRACT

Partial Trisomy 9q is a unique chromosomal anomaly with a distinctive phenotype. Only 5 cases have been reported in the literature till now. A large family with four affected children was studied in detail and was compared with the five previously reported cases. Determination of this novel balanced translocation in their family had helped us to offer prenatal diagnosis. This presentation is unique as even though partial trisomy 9q has been reported earlier with 9/17 translocations, our family is the first to have a translocation between q arms of chromosomes 9 and 17.


Subject(s)
Chromosomes, Human, Pair 17/genetics , Chromosomes, Human, Pair 9/genetics , Humans , Infant, Newborn , Karyotyping , Male , Pedigree , Phenotype , Translocation, Genetic , Trisomy/genetics
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