Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.

Author:

Vianna-Morgante A M,Nozaki M J,Ortega C C,Coates V,Yamamura Y

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. The 24 fluorescence patterns of the human metaphase chromosomes-distinguishing characters and variability;Caspersson, T.; Lomakka, G.; Zech, L.;Hereditas,1971

2. Pericentric inversion of a number 15 chromosome in nine members of one family;Crandall, B.F.; Sparkes, R.S.;Cytogenetics,1970

3. Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the 'cri-du-chat' syndrome;Faed, M.J.W.; Marrian, V.J.; Robertson, J.; Robson, E.B.; Cook, P.J.L.;Cytogenetics,1972

4. Pericentric inversion of chromosome No. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals;Hauksdottir, H.; Halld6rsson, S.; Jensson, O.; Mikkelsen, M.; McDermott, A.;journal of Medical Genetics,1972

5. Pericentric inversion of a group C autosome: a study of three families;Jacobs, P.A.; Cruickshank, G.; Faed, M.J.W.; Frackiewicz, A.; Robson, E.B.; Harris, H.; Sutherland, I.;Annals of Human Genetics,1968

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