NID1-related autosomal dominant Dandy-Walker malformation with occipital cephalocele in three generations
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference11 articles.
1. Neuroimaging of dandy-walker malformation;Correa;Top. Magn. Reson. Imag.,2011
2. Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant dandy-walker malformation and occipital cephaloceles;Darbro;Hum. Mutat.,2013
3. Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies;D'Antonio;Ultrasound Obstet. Gynecol.,2016
4. Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome;D'Antonio;Ultrasound Obstet. Gynecol.,2016
5. Occipital encephalocele associated with Dandy-Walker malformation: a case-based review;Gutierrez;Child’s Nerv. Syst.,2022
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1. Nidogen in development and disease;Frontiers in Cell and Developmental Biology;2024-03-14
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