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De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism.
Bal, M; Schrander-Stumpel, C T; Meers, L E; Theunissen, P M; Hamers, A J; Wennekes, M J; Engelen, J J.
Affiliation
  • Bal M; Department of Molecular Cell Biology and Genetics, University Maastricht, The Netherlands.
Genet Couns ; 11(3): 221-7, 2000.
Article in En | MEDLINE | ID: mdl-11043430
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 2 / Chromosomes, Human, Pair 18 / Developmental Disabilities / Epilepsy / Face Limits: Humans / Infant / Male Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2000 Document type: Article Affiliation country: Netherlands
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 2 / Chromosomes, Human, Pair 18 / Developmental Disabilities / Epilepsy / Face Limits: Humans / Infant / Male Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2000 Document type: Article Affiliation country: Netherlands