Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Author:

Bogart M H,Bradshaw C L,Jones O W,Schanberger J E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. A familial reciprocal translocation between three chromosomes;Creasy, M.R.; Crolla, J.A.; Daker, M.G.;Humangenetik,1974

2. Partial trisomy 1 I in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13;Sanchez 0, Yunis JJ, Escobar J1;Humangenetik,1974

3. Familial translocation involving chromosomes 6, 14 and 20 identified by quinacrine fluorescence;Alderdice, P.W.; Miller, O.J.; Miller, D.A.; Breg, W.R.; Gendel, E.; Zelson, C.;Humangenetik,1971

4. A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility;Joseph, A.; Thomas, I.M.;J Med Genet,1982

5. Possible complex translocation t(9; 14; 13)(ql2; pl?; q31) in mother of a child with 9ptrisomy syndrome;Fujita, H.; Abe, T.; Yamamoto, K.; Furuyama, J.I.;Humangenetik,1974

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