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Cheon, Chong‐Kun
15  Ergebnisse:
Personensuche X
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1

Clinical, endocrinological, and molecular features of four ..:

Lee, Yena ; Choi, Jin-Ho ; Oh, Arum...
Annals of Pediatric Endocrinology & Metabolism.  25 (2020)  2 - p. 97-103 , 2020
Link: https://doi.org/10.6065/..
 
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2

A rare case of multiple pituitary adenomas in an adolescent..:

Song, Ji-Yeon ; Mun, Sue-Jean ; Sung, Soon-Ki...
Annals of Pediatric Endocrinology & Metabolism.  22 (2017)  3 - p. 197-202 , 2017
Link: https://doi.org/10.6065/..
 
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3

NEU1 Mutation in a Korean Infant with Type 2 Sialidosis Pre..:

Lee, Yeoun-Joo ; Son, Seung-Kook ; Park, Jae-Hong..
Pediatrics & Neonatology.  56 (2015)  1 - p. 68-69 , 2015
Link: https://doi.org/10.1016/..
 
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4

Unravelling the mechanism of action of enzyme replacement t..:

Ko, Younhee ; Lee, CheolHo ; Moon, Myeong Hee...
Journal of Human Genetics.  61 (2015)  2 - p. 143-149 , 2015
Link: https://doi.org/10.1038/..
 
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5

The First Korean Case of HDR Syndrome Confirmed by Clinical..:

Cheon, Chong-Kun ; Kim, Gu-Hwan ; Yoo, Han-Wook
Yonsei Medical Journal.  56 (2015)  1 - p. 300 , 2015
Link: https://doi.org/10.3349/..
 
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6

Kabuki syndrome: clinical and molecular characteristics:

Cheon, Chong-Kun ; Ko, Jung Min
Korean Journal of Pediatrics.  58 (2015)  9 - p. 317 , 2015
Link: https://doi.org/10.3345/..
 
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7

Vitamin D receptor gene polymorphisms and type 1 diabetes m..:

Cheon, Chong‐Kun ; Nam, Hyo‐Kyoung ; Lee, Kee‐Hyoung...
Pediatrics International.  57 (2015)  5 - p. 870-874 , 2015
Link: https://doi.org/10.1111/..
 
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8

Clinical outcomes and the mutation spectrum of the OTC gene..:

Choi, Jin-Ho ; Lee, Beom Hee ; Kim, Ja Hye...
Journal of Human Genetics.  60 (2015)  9 - p. 501-507 , 2015
Link: https://doi.org/10.1038/..
 
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9

OTC Gene in Ornithine Transcarbamylase Deficiency: Clinical..:

Lee, Jung Hyun ; Kim, Gu-Hwan ; Yoo, Han-Wook.
Pediatric Neurology.  51 (2014)  3 - p. 354-359.e1 , 2014
Link: https://doi.org/10.1016/..
 
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10

The common exon 3 polymorphism of the growth hormone recept..:

Ko, Jung Min ; Kim, Jae‐Min ; Cheon, Chong‐Kun...
Clinical Endocrinology.  72 (2010)  2 - p. 196-202 , 2010
Link: https://doi.org/10.1111/..
 
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11

A case of Antley-Bixler syndrome caused by compound heteroz..:

Ko, Jung Min ; Cheon, Chong-Kun ; Kim, Gu-Hwan.
European Journal of Pediatrics.  168 (2008)  7 - p. 877-880 , 2008
Link: https://doi.org/10.1007/..
 
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12

Clinical, endocrinological, and molecular features of four ..:

Yena Lee ; Jin-Ho Choi ; Arum Oh...
http://e-apem.org/upload/pdf/apem-1938152-076.pdf.  , 2020
Link: https://doi.org/10.6065/..
 
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13

A rare case of multiple pituitary adenomas in an adolescent..:

Ji-Yeon Song ; Sue-Jean Mun ; Soon-Ki Sung...
http://e-apem.org/upload/pdf/apem-2017-22-3-197.pdf.  , 2017
Link: https://doi.org/10.6065/..
 
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14

NEU1 Mutation in a Korean Infant with Type 2 Sialidosis Pre..:

Yeoun-Joo Lee ; Seung-Kook Son ; Jae-Hong Park..
http://www.sciencedirect.com/science/article/pii/S1875957214001302.  , 2015
Link: https://doi.org/10.1016/..
 
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15

Kabuki syndrome: clinical and molecular characteristics:

Chong-Kun Cheon ; Jung Min Ko
http://kjp.or.kr/upload/pdf/kjped-58-317.pdf.  , 2015
Link: https://doi.org/10.3345/..
 
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