Accueil › Products › 16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridation (array CGH) in persistent pulmonary hypertension of the newborn

16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridation (array CGH) in persistent pulmonary hypertension of the newborn

Catégorie : Syndrome Microdélétion

16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridation (array CGH) in persistent pulmonary hypertension of the newborn

Produits similaires

Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychological and language phenotypes

A measurement of the ratio of the W and Z cross sections with exactly one associated jet in pp collisions at √es=7 TeV with ATLAS

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations