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Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing‐over
Author(s) -
KOSKEWESTPHAL THEA,
PRUSZAKSEEL ROSWITH E.,
NISS R.,
PASSARGE E.
Publication year - 1978
Publication title -
annals of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 77
eISSN - 1469-1809
pISSN - 0003-4800
DOI - 10.1111/j.1469-1809.1978.tb01898.x
Subject(s) - chromosomal inversion , trisomy , synapsis , recombination , partial trisomy , biology , chromosomal crossover , genetics , inversion (geology) , heterozygote advantage , long arm , chromosome , karyotype , allele , paleontology , gene , structural basin
SUMMARY Two unrelated infants with partial trisomy 13 for the distal half of the long arm are described. In one, a familial pericentric inversion is present in three generations and crossing‐over in the inversion loop is considered as cause of partial trisomy 13. The other showed a tandem duplication of the distal half of the long arm of chromosome 13 beyond 13q14. This is interpreted to have arisen by unequal crossing‐over in mispaired synapsis. It is suggested that recombination rather than breaks is a distinctive although rare cause of human chromosomal imbalance.