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T J Cho

Showing results (41-50 of 45) with videos related to

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Journal of Human Genetics|August 3, 1999
Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostosesK J Park, K H Shin, J L Ku, et al.
Clinical Genetics|June 8, 2012
Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locusS K Holman, T Morgan, G Baujat, et al.
Journal of Food Protection|November 29, 2015
Changes in the Microbial Composition of Microbrewed Beer during the Process in the Actual Manufacturing LineS A Kim, S H Jeon, N H Kim, et al.
Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et alF S Kaplan, M Xu, G Feldman, et al.
Journal of Medical Genetics|June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia familyJ Dai, O-H Kim, T-J Cho, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Journal of Human Genetics|August 3, 1999
Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostosesK J Park, K H Shin, J L Ku, et al.
Clinical Genetics|June 8, 2012
Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locusS K Holman, T Morgan, G Baujat, et al.
Journal of Food Protection|November 29, 2015
Changes in the Microbial Composition of Microbrewed Beer during the Process in the Actual Manufacturing LineS A Kim, S H Jeon, N H Kim, et al.
Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et alF S Kaplan, M Xu, G Feldman, et al.
Journal of Medical Genetics|June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia familyJ Dai, O-H Kim, T-J Cho, et al.
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