Microcephaly
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- 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