E. Pandelia

Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter.

D. Vassilopoulos, K. Brøndum‐Nielsen, G. Kitsos, 1997, American journal of medical genetics.

Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16

R. Tenconi, G. Neri, S. Savasta, 2007, Human Genetics.

Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction

G. Karadima, D. Vassilopoulos, M. Petersen, 1999, Clinical genetics.

Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non‐acrocentric satellited chromosomes

Z. Tümer, N. Moschonas, S. Douzgou, 2011, American journal of medical genetics. Part A.

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy

M. Qumsiyeh, S. K. Rafi, J. Gyftodimou, 2003, American journal of medical genetics. Part A.

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face

K. Mrasek, Y. Gyftodimou, M. Petersen, 2006, Cytogenetic and Genome Research.

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11

C. Petit, D. Weil, T. Yang, 2008, Clinical genetics.