1. Trisomy 22: A clinical identifiable phenotype;Alfi;Birth Defects: Original Article Series,1975
2. Deux cas de trisomie 1 lq(231→qter) par translocation t(11;22)q(231;q 111) dans deux families differentes;Aurias;Ann. Genet.,1975
3. Trisomie Hq(q23→qt34) par translocation maternelle t(11;22)- (q23.1;q11.1)(q23.1;q11.1);Ayraud;Ann. Genet.,1976
4. Probable trisomy 22 identified by fluorescent and trypsin Giemsa banding;Bass;Ann. Genet.,1973
5. Two successive partial trisomies for opposite halves of chromosome 22 in a mother with a balanced translocation;Bendel;J. Med. Genet.,1982