S. Nusbaum

Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy

J. Steffann, M. Vekemans, L. Colleaux, 2016, Clinical genetics.

Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature

E. Bourel-ponchel, C. Rooryck, D. Lacombe, 2015, American journal of medical genetics. Part A.

Recurrent partial trisomy 1q22-q44 in clonal intraepithelial lymphocytes in refractory celiac sprue.

E. Macintyre, N. Brousse, S. Romana, 2003, Gastroenterology.

LRRFIP1, a new FGFR1 partner gene associated with 8p11 myeloproliferative syndrome

S. Romana, M. Vekemans, I. Radford‐Weiss, 2009, Leukemia.

Post-allogeneic haematopoietic stem cell transplantation membranous nephropathy: clinical presentation, outcome and pathogenic aspects.

B. Knebelmann, C. Combe, F. Glowacki, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

FISH detection of chromosome 14q32/IgH translocations: evaluation in follicular lymphoma

E. Macintyre, M. Vekemans, I. Radford‐Weiss, 1998, British journal of haematology.