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Microcephaly
1Q21.1 Duplication Syndrome and Epilepsy Case Report and Review
Megalencephaly and Macrocephaly
South Carolina Birth Defects Program Resource Guide
Endosomal Trafficking Defects Alter Neural Progenitor Proliferation And
Proximal Microdeletions and Microduplications of 1Q21.1 Contribute to Variable Abnormal Phenotypes
Miller–Dieker Syndrome, Type 1 Lissencephaly
AKT3 Gene AKT Serine/Threonine Kinase 3
Syndromes with Lissencephaly
Microcephaly Microcephaly Is a Condition Where a Baby’S Head Is Much Smaller Than Expected
NBDPN Abstractor's Instructions
Blueprint Genetics Polymicrogyria Panel
Dandy–Walker Malformation: an Incidental Finding Case Report
Fact Sheet Virginia Genetics Program 1-800-523-4019
Clinical Phenotype of the Recurrent 1Q21.1 Copy-Number Variant
Cystic Leukoencephalopathy Without Megalencephaly
Dissecting Molecular Genetic Mechanisms of 1Q21.1 CNV in Neuropsychiatric Disorders
6 Tips on Zika for Pediatricians
Pediatric Neurosurgical Disease
Top View
Migrasjonsforstyrrelser Og Pontocerebellær Hypoplasi
1Q21.1 Deletion Syndrome
Screening, Assessment and Management of Neonates And
In-Depth Investigations of Adolescents and Adults with Holoprosencephaly Identify Unique Characteristics
Appendix 3.5 Case Inclusion Guidance for Potentially Zika-Related Birth Defects
Surveillance of Microcephaly Webinar Transcript
Holoprosencephaly
Congenital Infectious Encephalopathies
Evaluation and Management of Children with Holoprosencephaly
Two Cases with Microcephaly, Polymicrogyria, and Cerebellar Malformations
Cephaloceles and Related Malformations
Holoprosencephaly Classified by Computed Tomography
Developmental Posterior Fossa Abnormalities with Associated
The Presence of Two Rare Genomic Syndromes, 1Q21 Deletion and Xq28 Duplication, Segregating Independently in a Family with Intellectual Disability
Congenital Microcephaly
Microcephaly
1Q21.1 Microdeletion
Macrocephaly, Increased Intracranial Pressure, and Hydrocephalus in the Infant and Young Child Alexandra T