Volume 4, Number 4, Year 2015

Original Articles
Hela Ben Khelifa, Molka Kammoun, Hanene Hannachi, Najla Soyah, Saber Hammami, Hatem Elghezal, Damien Sanlaville, Ali Saad, and Soumaya Mougou-Zerelli
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits

Hakan Cangul, Banu K. Aydin, and Firdevs Bas
A Homozygous TPO Gene Duplication (c.1184_1187dup4) Causes Congenital Hypothyroidism in Three Siblings Born to a Consanguineous Family

Case Reports
Marine Manvelyan, Izabella Simonyan, Galina Hovhannisyan, Rouben Aroutiounian, Ahmed B. Hamid, and Thomas Liehr
A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement

Paldeep S. Atwal and C. Macmurdo
UA Case of Concurrent Miller-Dieker Syndrome (17p13.3 Deletion) and 22q11.2 Deletion Syndrome

Leonardo I. Valentin, Luis Perez, and Prakash Masand
Hepatoblastoma Associated with Trisomy 18

Paldeep S. Atwal
A Case of Anterior Segment Dysgenesis with Iridolenticular Adhesions in Trisomy 18