Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3)

Author:

Asano Takeshi,Ikeuchi Tatsuro,Shinohara Tamiko,Enokido Hisashi,Hashimoto Kiyoshi

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference29 articles.

1. Andrews, T., Gardiner, A.C. and Boon, A.R. 1982. Recombinant chromosome 18 in two offspring of a chromosome 18 inversion heterozygote.Ann. Génét. 25, 185–188.

2. Borovik, C.L., Brunoni, D., Sato, A.E., Stavále, J.N., Cardoso, S.H., Montezzo, L.C. and Perez, A.B.A. 1987. Holoprosencephaly as a result of unbalanced familial translocation rep(7;18) (q36;q21).Rev. Brazil. Genet. 10: 269–276.

3. De Grouchy, J. and Turleau, C. 1977.Clinical Atlas of Human Chromosomes. A Wiley Medical Publication, John Wiley & Sons, New York, Chichester, Brisbane, Toronto, pp. 159–183.

4. De Torres, L., Ferrer, A.S. and Abrisqueta, J.A. 1984. Partial trisomy 18 due to a maternal translocation t(9;18).Hum. Genet. 68: 272.

5. Faust, J., Habedank, M. and Nieuwenhuijsen, C. 1976. The 18p-syndrome. Report of four cases.Eur. J. Pediatr. 123: 59–66.

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