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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Seizures and NRXN3[original query]
Copy number variation in a hospital-based cohort of children with epilepsy.
Epilepsia open 2017 Jun 2 (2): 244-254.
Vlaskamp Danique R M, Callenbach Petra M C, Rump Patrick, Giannini Lucia A A, Dijkhuizen Trijnie, Brouwer Oebele F, van Ravenswaaij-Arts Conny M
Application of Chromosome Microarray Analysis in the Investigation of Developmental Disabilities and Congenital Anomalies: Single Center Experience and Review of NRXN3 and NEDD4L Deletions.
Molecular syndromology 2020 11 11 (4): 197-206.
Çebi Alper Han, Alt?ner ?u
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