Lee CL - Search Results

1

Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome.

Lin HY, Lee CL, Fran S, Tu RY, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Tsai MC, Chao MC, Tsai LP, Yang CF, Su PH, Pan YW, Lee CH, Chu TH, Chuang CK, Lin SP. Lin HY, et al. Among authors: lee ch, lee cl. J Pers Med. 2021 Nov 13;11(11):1197. doi: 10.3390/jpm11111197. J Pers Med. 2021. PMID: 34834549 Free PMC article.

2

Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay.

Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. Chen CP, et al. Among authors: lee cl. Taiwan J Obstet Gynecol. 2017 Feb;56(1):93-97. doi: 10.1016/j.tjog.2016.12.002. Taiwan J Obstet Gynecol. 2017. PMID: 28254235 Free article.

3

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.

Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. Chen CP, et al. Among authors: lee cl. Taiwan J Obstet Gynecol. 2017 Feb;56(1):98-101. doi: 10.1016/j.tjog.2016.12.003. Taiwan J Obstet Gynecol. 2017. PMID: 28254236 Free article.

4

Functional independence of Taiwanese children with Prader-Willi syndrome.

Lee CL, Lin HY, Tsai LP, Chiu HC, Tu RY, Huang YH, Chien YH, Lee NC, Niu DM, Chao MC, Tsai FJ, Chou YY, Chuang CK, Lin SP. Lee CL, et al. Among authors: lee nc. Am J Med Genet A. 2018 Jun;176(6):1309-1314. doi: 10.1002/ajmg.a.38705. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696774

5

Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21-year period.

Lin HY, Chuang CK, Lee CL, Tu RY, Lo YT, Chiu PC, Niu DM, Fang YY, Chen TL, Tsai FJ, Hwu WL, Lin SJ, Chang TM, Lin SP. Lin HY, et al. Among authors: lee cl. Am J Med Genet A. 2018 Sep;176(9):1799-1809. doi: 10.1002/ajmg.a.40351. Epub 2018 Aug 2. Am J Med Genet A. 2018. PMID: 30070758

6

The relationships between urinary glycosaminoglycan levels and phenotypes of mucopolysaccharidoses.

Lin HY, Lee CL, Lo YT, Wang TJ, Huang SF, Chen TL, Wang YS, Niu DM, Chuang CK, Lin SP. Lin HY, et al. Among authors: lee cl. Mol Genet Genomic Med. 2018 Nov;6(6):982-992. doi: 10.1002/mgg3.471. Epub 2018 Sep 16. Mol Genet Genomic Med. 2018. PMID: 30296009 Free PMC article.

7

Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.

Lee CL, Lee CH, Chuang CK, Chiu HC, Chen YJ, Chou CL, Wu PS, Chen CP, Lin HY, Lin SP. Lee CL, et al. Among authors: lee ch. Pediatr Neonatol. 2019 Aug;60(4):453-460. doi: 10.1016/j.pedneo.2018.11.006. Epub 2018 Nov 27. Pediatr Neonatol. 2019. PMID: 30581099 Free article.

8

Long-term outcomes of enzyme replacement therapy for Taiwanese patients with Mucopolysaccharidosis I.

Lin HY, Lee CL, Chuang CK, Lin SP. Lin HY, et al. Among authors: lee cl. Pediatr Neonatol. 2019 Oct;60(5):577-578. doi: 10.1016/j.pedneo.2019.05.005. Epub 2019 May 29. Pediatr Neonatol. 2019. PMID: 31196723 Free article. No abstract available.

9

Functional independence of Taiwanese patients with mucopolysaccharidoses.

Lee CL, Lin HY, Chuang CK, Chiu HC, Tu RY, Huang YH, Hwu WL, Tsai FJ, Chiu PC, Niu DM, Chen YJ, Chao MC, Chang TM, Lin JL, Chang CY, Kao YC, Lin SP. Lee CL, et al. Mol Genet Genomic Med. 2019 Aug;7(8):e790. doi: 10.1002/mgg3.790. Epub 2019 Jun 18. Mol Genet Genomic Med. 2019. PMID: 31215158 Free PMC article.

10

An At-Risk Population Screening Program for Mucopolysaccharidoses by Measuring Urinary Glycosaminoglycans in Taiwan.

Lin HY, Lee CL, Lo YT, Tu RY, Chang YH, Chang CY, Chiu PC, Chang TM, Tsai WH, Niu DM, Chuang CK, Lin SP. Lin HY, et al. Among authors: lee cl. Diagnostics (Basel). 2019 Oct 5;9(4):140. doi: 10.3390/diagnostics9040140. Diagnostics (Basel). 2019. PMID: 31590383 Free PMC article.

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