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Reciprocal syndromes caused by deficiency duplication resulting from maternal t (10;18) (p12;q22) translocation

Rethoré, M.O.; Prieur, M.; de Blois, M.C.; Naffah, J.; Ravel, A.; Villain, E.; Lejeune, J.

Annales de Genetique 28(3): 149-153

1985

ISSN/ISBN: 0003-3995
PMID: 3879147
Document Number: 255465
The detection of a familial translocation, t(10;18)(p12;q22), has made possible the observation in type and countertype of two related persons with opposite chromosomal imbalance: trisomy 18q22----18qter with monosomy 10p12----10pter in one of the two and monosomy 18q22----10pter in the other. In each case the abnormalities attributable to monosomy overrule those attributable to monosomy overrule those attributable to the associated trisomy.

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