M. C. Balcı Et Al. , "RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY," 43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri , İstanbul, Turkey, pp.293-294, 2021
Balcı, M. C. Et Al. 2021. RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY. 43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri , (İstanbul, Turkey), 293-294.
Balcı, M. C., Körbeyli, H. K., & Gökçay, G. F., (2021). RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY . 43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri (pp.293-294). İstanbul, Turkey
Balcı, Mehmet, Hüseyin Kutay KÖRBEYLİ, And Gülden Fatma GÖKÇAY. "RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY," 43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri, İstanbul, Turkey, 2021
Balcı, Mehmet C. Et Al. "RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY." 43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri , İstanbul, Turkey, pp.293-294, 2021
Balcı, M. C. Körbeyli, H. K. And Gökçay, G. F. (2021) . "RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY." 43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri , İstanbul, Turkey, pp.293-294.
@conferencepaper{conferencepaper, author={Mehmet Cihan BALCI Et Al. }, title={RARE HERITAGE METABOLIC DISEASE IN THE DIFFERENTIAL DIAGNOSIS OF TREATMENT-RESISTANT SKIN LESIONS: PROLIDASE DEFICIENCY}, congress name={43. Pediatri Günleri ve 22.Pediatri Hemşireliği Günleri}, city={İstanbul}, country={Turkey}, year={2021}, pages={293-294} }