TY - GEN AU - Tutunculer,Filiz AU - Darendeliler,Feyza AU - Gunoz,Hulya AU - Karaman,Birsen AU - Kayserili,Hulya TI - 18q deletion syndrome associated with autoimmune thyroid disease presenting as hyperthyroidism SN - 0334-018X PY - 2005///0705 KW - Autoimmune Diseases KW - diagnosis KW - Chromosomes, Human, Pair 18 KW - Diagnosis, Differential KW - Female KW - Gene Deletion KW - Humans KW - Hypothyroidism KW - Infant KW - Syndrome N1 - Publication Type: Case Reports; Letter UR - https://doi.org/10.1515/jpem.2005.18.4.419 ER -