Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

Author:

Dawson A J,Mears A J,Chudley A E,Bech-Hansen T,McDermid H

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference21 articles.

1. Site-specific reciprocal translocation, t(ll; 22)(q23; ql 1), in several unrelated families with 3: 1 meiotic disjunction;Zackai, E.H.; Emanuel, B.S.;Am J Med Genet,1980

2. The 1 Iq; 22q translocation: a European collaborative analysis of 43 cases;Fraccaro, M.; Lindsten, J.; Ford, C.E.;Hum Genet,1980

3. The 11 q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 families;Iselius, L.; Lindsten, J.; Aurias, A.;Hum Genet,1983

4. Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(1l; 22)(q23; qll);Martin, R.H.;Clin Genet,1984

5. Unusual segregation for 1 q22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid;Soler, A.; Carrio, A.; Perez-Vidal, M.T.; Borrell, A.; Fortuny, A.,1993

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