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4 in total

1. Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.

Authors: T H Shaikh; M L Budarf; L Celle; E H Zackai; B S Emanuel
Journal: Am J Hum Genet Date: 1999-12 Impact factor: 11.025

2. Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors: S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal: Am J Hum Genet Date: 2000-08-08 Impact factor: 11.025

3. A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.

Authors: Vaidehi Jobanputra; Wendy K Chung; April M Hacker; Beverly S Emanuel; Dorothy Warburton
Journal: Prenat Diagn Date: 2005-08 Impact factor: 3.050

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

Authors: A J Dawson; A J Mears; A E Chudley; T Bech-Hansen; H McDermid
Journal: J Med Genet Date: 1996-11 Impact factor: 6.318

4 in total