A. Hacker

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

Alexander Eckehart Urban, Mark B Gerstein, Todd Richmond, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum.

B. Emanuel, M. I. Melaragno, M. Cernach, 2008, European journal of medical genetics.

Interrupted aortic arch type B in A patient with cat eye syndrome.

B. Emanuel, M. Cernach, S. Belangero, 2009, Arquivos brasileiros de cardiologia.

A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies.

A. Gotter, L. Medne, B. Emanuel, 2007, Genome research.

Deletion 22q11.2: Report of a complex meiotic mechanism of origin

M. Cernach, D. Christofolini, L. Kulikowski, 2007, American journal of medical genetics. Part A.

Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.

T. Shaikh, B. Emanuel, S. Saitta, 2007, Genome research.

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.

E. Zackai, B. Emanuel, S. Saitta, 2004, Human molecular genetics.

Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.

B. Emanuel, H. Kurahashi, T. Glover, 2014, Cancer genetics.

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

E. Rappaport, J. Vorstman, A. Hacker, 2006, Human mutation.

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

V. Jobanputra, W. Chung, D. Warburton, 2005, Prenatal diagnosis.

A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).

E. Zackai, C. Haldeman-Englert, T. Shaikh, 2010, American journal of human genetics.