[Partial deletion of short arms in chromosomes from group B with translocation to group D in the father of children with multiple developmental anomalies].
D000328:Adult; D002872:Chromosome Deletion; D002900:Chromosomes, Human, 1-3; D002905:Chromosomes, Human, 4-5; D003410:Cri-du-Chat Syndrome / Q000235:genetics*; D005260:Female; D006801:Humans; D007223:Infant; D008297:Male; D014178:Translocation, Genetic
Cześciowa delecja ramion krótkich chromosomów z grupy B z przemieszczeniem do grupy D u ojca dzieci z mnogimi wadami rozwojowymi.