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

Résumé

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.


Sujets)
Chromosomes humains de la paire 17/génétique , Chromosomes humains de la paire 9/génétique , Humains , Nouveau-né , Caryotypage , Mâle , Pedigree , Phénotype , Translocation génétique , Trisomie/génétique
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