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Clin Genet ; 25(1): 52-8, 1984 Jan.
Article in English | MEDLINE | ID: mdl-6705241

ABSTRACT

The phenotype of a boy with monosomy of a small segment of chromosome (10) (q24.2----q25.3) is described. In his family a balanced insertion (5;10) is found in three generations. Moreover there are two persons who are trisomic for the same small segment of chromosome 10 for which the boy is monosomic.


Subject(s)
Chromosome Aberrations/genetics , Chromosome Deletion , Chromosomes, Human, 4-5/ultrastructure , Chromosomes, Human, 6-12 and X/ultrastructure , Intellectual Disability/genetics , Abnormalities, Multiple/genetics , Chromosome Disorders , Chromosome Fragility , Chromosomes, Human, 16-18/ultrastructure , Humans , Infant , Male , Pedigree , Translocation, Genetic , Trisomy
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