Jung-Min Ko, Ph.D.

Affiliations: 
2001 University of Texas at Austin, Austin, Texas, U.S.A. 
Area:
Bilingual and Multicultural Education, Speech Communication, Adult and Continuing Education
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Diane L. Schallert grad student 2001 UT Austin
 (The effect of negotiation of meaning on the storytelling of adult students in ESL classrooms.)
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Publications

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Lee SH, Ko JM, Song MK, et al. (2020) A Korean child diagnosed with malonic aciduria harboring a novel start codon mutation following presentation with dilated cardiomyopathy. Molecular Genetics & Genomic Medicine. e1379
Bang E, Kim YE, Ko JM, et al. (2020) Lentigo Maligna in a Patient with Xeroderma Pigmentosum, Variant type: A case report with dermoscopic findings and review of the literature. Photodermatology, Photoimmunology & Photomedicine
Lee Y, Park S, Lee JS, et al. (2020) Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population. Scientific Reports. 10: 1413
Lim C, Jung ST, Shin CH, et al. (2019) Diagnosis and Management of Hip Dislocation in Patients with Kabuki Syndrome. Clinics in Orthopedic Surgery. 11: 474-481
Ryu J, Ko JM, Shin CH. (2019) A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-up. Bmc Medical Genetics. 20: 188
Kim BY, Ko JM, Park MH, et al. (2019) Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation. Stem Cell Research. 41: 101622
Park HJ, Ko JM, Lim J, et al. (2019) American consumers' perception and acceptance of an ethnic food with strong flavor: A case study of Kimchi with varying levels of red pepper and fish sauce. Journal of the Science of Food and Agriculture
Fiordaliso SK, Iwata-Otsubo A, Ritter AL, et al. (2019) Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment. American Journal of Human Genetics
Han SR, Lee YA, Shin CH, et al. (2019) Clinical and Molecular Characteristics of GNAS Inactivation Disorders Observed in 18 Korean Patients. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association
Choi N, Ko JM, Shin SH, et al. (2019) Phenotypic and Genetic Characteristics of Five Korean Patients with Costello Syndrome. Cytogenetic and Genome Research
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