Ohcanbohtosat - Jung Sook Ha
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CASK Mutation in an Infant with Microcephaly, Pontocerebellar Hypoplasia, and Hearing Loss Dahkki Jun Chul Byun, Jung Sook Ha
Almmustuhtton 2022Hildobáiki: Láddejuvvo…Connect to this object online.
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A sporadic case of Loeys-Dietz syndrome type I with two novel mutations of the gene Dahkki Jung Sook Ha, Yeo Hyang Kim
Almmustuhtton 2011Hildobáiki: Láddejuvvo…Connect to this object online.
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3
TSEN54 Gene-Related Pontocerebellar Hypoplasia Type 2 in a Newborn with Refractory Myoclonic Seizures Dahkki Jun Chul Byun, Jung Sook Ha, Chun Soo Kim
Almmustuhtton 2022Hildobáiki: Láddejuvvo…Connect to this object online.
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4
The Effect of <i>NUDT15</i>, <i>TPMT</i>, <i>APEX1</i>, and <i>ITPA</i> Genetic Variations on Mercaptopurine Treatment of Pediatric Acute Lymphoblastic Leukemia Dahkki Jae Min Lee, Ye Jee Shim, Do-Hoon Kim, Nani Jung, Jung-Sook Ha
Almmustuhtton 2021Hildobáiki: Láddejuvvo…Connect to this object online.
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5
Diagnosis of Duchenne Muscular Dystrophy in a Presymptomatic Infant Using Next-Generation Sequencing and Chromosomal Microarray Analysis: A Case Report Dahkki Eun-Woo Park, Ye-Jee Shim, Jung-Sook Ha, Jin-Hong Shin, Soyoung Lee, Jang-Hyuk Cho
Almmustuhtton 2021Hildobáiki: Láddejuvvo…Connect to this object online.
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The first Korean case with Floating-Harbor syndrome with a novel mutation diagnosed by targeted exome sequencing Dahkki Eun Mi Choi, Dong Hyun Lee, Seok Jin Kang, Ye Jee Shim, Heung Sik Kim, Jun Sik Kim, Jong In Jeong, Jung-Sook Ha, Ja-Hyun Jang
Almmustuhtton 2018Hildobáiki: Láddejuvvo…Connect to this object online.
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