A case of partial trisomy 22 resulting from maternal 11/22 translocation

Author:

Narahara Kouji,Kodama Yoshifumi,Kimura Shunsuke,Kamoi Motoji,Inoue Hideo,Kimoto Hiroshi

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference31 articles.

1. Alfi, O.S., Sanger, R.G., and Donnell, G.M. 1975. Trisomy 22: a clinically identifiable syndrome. Birth Defects Original Article Series 11(5):241–245.

2. Bass, H.N., Crandall, B.F., and Sparkes, R.S. 1973. Probable trisomy 22 identified by fluorescent and trypsin-geimsa banding.Ann. Génét. 16:189–192.

3. Begleiter, M.L., Kulkarni, P., and Harris, D.J. 1976. Confirmation of trisomy 22 by trypsin-giemsa staining.J. Med. Genet. 13:517–520.

4. Bofinger, M.K. and Soukup, S.W. 1977. Cat eye syndrome: partial trisomy 22 due to translocation in the mother.Am. J. Dis. Child. 131:893–897.

5. Borgaonkar, D.S., McKusick, V.A., and Farber, P.A. 1973. An inherited small extra chromosome: a mother with 46,XX,t(17;22) (p1?;q1?) and a son with 47,XY,+der(22)mat.J. Med. Genet. 10:379–384.

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