ÖNENLİ MUNGAN, H. N. Et Al. 2018. An interesting family: A cousin with carbonic anyhdrase deficiency type II together with Galloway-Mowat Syndrome and another two cousins with arginase deficiency.. 14th MEMG meeting , (ATİNA, Greece).

ÖNENLİ MUNGAN, H. N., KOR, D., BULUT, F. D., Şeker-Yılmaz, B., & KILAVUZ, S., (2018). An interesting family: A cousin with carbonic anyhdrase deficiency type II together with Galloway-Mowat Syndrome and another two cousins with arginase deficiency. . 14th MEMG meeting, ATİNA, Greece

ÖNENLİ MUNGAN, HALİSE Et Al. "An interesting family: A cousin with carbonic anyhdrase deficiency type II together with Galloway-Mowat Syndrome and another two cousins with arginase deficiency.," 14th MEMG meeting, ATİNA, Greece, 2018

ÖNENLİ MUNGAN, HALİSE N. Et Al. "An interesting family: A cousin with carbonic anyhdrase deficiency type II together with Galloway-Mowat Syndrome and another two cousins with arginase deficiency.." 14th MEMG meeting , ATİNA, Greece, 2018

ÖNENLİ MUNGAN, H. N. Et Al. (2018) . "An interesting family: A cousin with carbonic anyhdrase deficiency type II together with Galloway-Mowat Syndrome and another two cousins with arginase deficiency.." 14th MEMG meeting , ATİNA, Greece.

@conferencepaper{conferencepaper, author={HALİSE NESLİHAN ÖNENLİ MUNGAN Et Al. }, title={An interesting family: A cousin with carbonic anyhdrase deficiency type II together with Galloway-Mowat Syndrome and another two cousins with arginase deficiency.}, congress name={14th MEMG meeting}, city={ATİNA}, country={Greece}, year={2018}}