L1 syndrome
Top View
- Gene and Disease List
- Phenotypes and Variants in Cases Submitted for X-Linked Intellectual Disability (XLID) Gene Panel Testing
- Positive XL Female
- The Genetic Determinants of Cerebral Palsy
- Rare Disease Day
- Three Cases with L1 Syndrome and Two Novel Mutations in the L1CAM Gene
- UC Davis UC Davis Previously Published Works
- Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
- Molecular Biology of Pediatric Hydrocephalus and Hydrocephalus-Related Diseases
- Centoscreen® Carrier Screening DETECTS 332 AUTOSOMAL and X-LINKED RECESSIVE DISORDERS
- Expanded Carrier Screen Gene List (By Gene)
- Clinical, Genetic and Imaging Findings Identify New Causes for Corpus
- Preliminary Study of L1 Syndrome Patients With
- Characterizing the Phenotypic Effect of Xq28 Duplication Size in MECP2 Duplication Syndrome
- MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly
- Familly with Two Different Cases of Post-And Pre-Natal L1 Syndrome: When
- DISEASE 1 17-Beta-Hydroxysteroid Dehydrogenase Defciency
- A Novel Mutation in the L1CAM Gene: a Tale of Two Brothers