Syndrome Microdélétion

Affichage de 1–9 sur 14 résultats

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

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  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

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  Concurrent microdeletion and duplication of 22q11.2

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  Congenital heart disease is associated with reduced cortical and hippocampal volume in patients with 22q11.2 deletion syndrome

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

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  Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): A cross-sectional and longitudinal study

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  Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

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  Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome

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  Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) Syndrome