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Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2→q25.3)
Author(s) -
Vooren M. J. van de,
Planteydt H. T.,
Hagemeijer A.,
PetersSlough M. F.,
Timmerman M. J.
Publication year - 1984
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1984.tb00462.x
Subject(s) - monosomy , genetics , trisomy , chromosome 21 , aneuploidy , chromosome , biology , phenotype , chromosome 7 (human) , karyotype , gene
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.