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Your search keyword '"Aerssens P"' showing total 2 results
Start Over Author "Aerssens P" Topic chromosome deletion
2 results on '"Aerssens P"'

1. A de-novo 15q24.2 deletion involving SIN3A is associated with emotional, behavioural, motor problems and hypersensitivity in a girl with above average intelligence and typical facial features.

Author

Sleyp Y, Swillen A, Van Den Bogaert K, Massa G, Aerssens P, and Peeters H

Subjects
Child, Chromosomes, Human, Pair 15 genetics, Emotions, Facies, Female, Humans, Intelligence, Mental Disorders diagnosis, Mental Disorders genetics, Motor Disorders diagnosis, Motor Disorders genetics, Chromosome Deletion, Chromosome Disorders diagnosis, Chromosome Disorders genetics, Intellectual Disability diagnosis, Intellectual Disability genetics, Phenotype, Sin3 Histone Deacetylase and Corepressor Complex genetics
Published
2020
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2. The importance of excluding 13q deletion mosaicism in the diagnosis of retinoblastoma associated with dysmorphic features.

Author

Van Esch H, Aerssens P, and Fryns JP

Subjects
Child, Preschool, Diagnosis, Differential, Female, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Recurrence, Retinoblastoma Protein genetics, Chromosome Deletion, Chromosomes, Human, Pair 13 genetics, Face abnormalities, Mosaicism, Retinal Neoplasms diagnosis, Retinal Neoplasms genetics, Retinoblastoma diagnosis, Retinoblastoma genetics
Published
2005

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