Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

BALLABIO A;ANDRIA G;CARROZZO R;PERSICO G;BICK D;CAMPBELL L;ROPERS HH;FERGUSON SMITH MA;GIMELLI G;FRACCARO M;MARASCHIO, PAOLA;ZUFFARDI, ORSETTA;BARDONI B;GUIOLI S;CAMERINO, GIOVANNA

1989