Association of male XX with Pierre Robin syndrome in a child whose father has a balanced 46XY, t (16; 17) (p13;q21) translocation
Petrus, M.; Bourrouillou, G.; Dutau, G.; Colombies, P.; Rochiccioli, P.
Journal de Genetique Humaine 29(2): 191-196
1981
ISSN/ISBN: 0021-7743 PMID: 7199077 Document Number: 179760
The authors relate the association XX male and syndrome of Pierre Robin in a child whose father presents a reciprocal equilibrated translocation 46,XY t (16;17) (p13;q21). They discuss the possible relation between these different anomalies and notably the possibility of a genic effect.