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B Y Pyun 2 Articles
Original Article
11 q Deletion Syndrome.
Y B Im, S B Park, B Y Pyun, J O Park, S J Lee, S Y Moon
Clin Exp Pediatr. 1989;32(2):239-243.   Published online February 28, 1989
llq deletion syndrome is a rare chromosomal anomaly. The authors experienced a case of llq deletion syndrome with congenital glaucoma and infantile spasm in a female child. She showed delayed psychomotor development, flat occiput, hypertelorism, low set malformed ears, flat nasal bridge, short neck, simian line on right palm and throm. bocytopenia. Chromosomal study showed the deletion of the long arm of chromosme 11, karyotypically...
Case Report
A case of Pneumothorax due to Paragonimiasis with Family.
S J Han, B Y Pyun, D H Lee, S J Lee
Clin Exp Pediatr. 1982;25(2):168-174.   Published online February 28, 1982
We experienced one case of pneumothorax due to paragonimiasis of 6 years aged girl. The diagnosis was established by characteristic feature of ova on stool and sputum. A brief review of related literature was presented.
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