This paper reports a large kinship with a familial (21; 22) translocation occurring in both the
balanced and the unbalanced states. Recurrence risks for the (21; 22) translocation in the …

FAMILIAL 21/22 TRANSLOCATION Page 1 FAMILIAL 21/22 TRANSLOCATION Z. PAPP, B.
DOLHAY, S. GARDO Human Genetics Laboratory, Department of Obstetrics and …

Follow-Up Investigation of a Familial Translocation 14/18 | Acta geneticae medicae et
gemellologiae: twin research | Cambridge Core Skip to main content Accessibility help We use …

We have detected eight patients with a single metaphase having a 7/14 translocation. In all
cases, the breakpoint on chromosome 14 was 14q12, while the breakpoint on chromosome …

A family showing a complex translocation between chromosomes 7, 8, and 9 with
breakpoints at 7q21, 7q33, 8p23, and 9p23 is described. The proband had been referred …

A familial Robertsonian translocation 15/22 was ascertained through a female carrier whose
four pregnancies ended in missed abortions. Eleven 15/22 translocation carriers were …

TRANSLOCATION of chromosome 21 to another chromosome, usually a D-or G-group
chromosome, is a well-recognized cause for familial mongolism. 1 The greatly increased risk …

Segregation analysis of the offspring of balanced translocation carriers was performed on
327 pedigrees collated from published sources and personal communications. Correction …

A dicentric translocation is described involving chromosomes 13 and 18 in which the
centromere of chromosome 13 was suppressed. The translocation was ascertained by …

FIG. 5. Karyotype of mother, II. 7. following results: the grandfather II, the father II. 7, and the
female sib III. io were normal. Anomaly was present in the others, the grandmother I. 2, the …