Lin JL - Search Results

1

Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature.

Lo FS, Lin JL, Kuo MT, Chiu PC, Shu SG, Chao MC, Lee YJ, Lin SP. Lo FS, et al. Among authors: lin jl, lin sp. Eur J Pediatr. 2009 Aug;168(8):919-23. doi: 10.1007/s00431-008-0858-z. Epub 2008 Oct 29. Eur J Pediatr. 2009. PMID: 18958496 Review.

2

Novel point mutations in complete androgen insensitivity syndrome with incomplete müllerian regression: two Taiwanese patients.

Van YH, Lin JL, Huang SF, Luo CC, Hwang CS, Lo FS. Van YH, et al. Among authors: lin jl. Eur J Pediatr. 2003 Nov;162(11):781-4. doi: 10.1007/s00431-003-1301-0. Epub 2003 Sep 17. Eur J Pediatr. 2003. PMID: 13680382

3

Asplenia syndrome in a pair of monozygotic twins.

Hwang MS, Su WJ, Lin JL. Hwang MS, et al. Among authors: lin jl. Acta Paediatr. 2006 Apr;95(4):500-1. doi: 10.1080/08035250500377802. Acta Paediatr. 2006. PMID: 16720503

4

Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome.

Hung CS, Lin JL, Lee YJ, Lin SP, Chao MC, Lo FS. Hung CS, et al. Among authors: lin jl, lin sp. J Formos Med Assoc. 2007 Feb;106(2):169-72. doi: 10.1016/S0929-6646(09)60235-7. J Formos Med Assoc. 2007. PMID: 17339163 Free article.

5

Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndrome.

Lin HY, Lin SP, Tsai LP, Chao MC, Chen MR, Chuang CK, Huang CY, Tsai FJ, Chou IC, Chiu PC, Huang CH, Yen JL, Lin JL, Kuo PL. Lin HY, et al. Among authors: lin jl, lin sp. J Chin Med Assoc. 2008 Jun;71(6):305-9. doi: 10.1016/S1726-4901(08)70127-8. J Chin Med Assoc. 2008. PMID: 18567561 Free article.

6

Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004.

Lin HY, Lin SP, Chuang CK, Niu DM, Chen MR, Tsai FJ, Chao MC, Chiu PC, Lin SJ, Tsai LP, Hwu WL, Lin JL. Lin HY, et al. Among authors: lin sj, lin jl, lin sp. Am J Med Genet A. 2009 May;149A(5):960-4. doi: 10.1002/ajmg.a.32781. Am J Med Genet A. 2009. PMID: 19396827

7

Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in Taiwan.

Cheng KH, Liu MY, Kao CH, Chen YJ, Hsiao KJ, Liu TT, Lin HY, Huang CH, Chiang CC, Ho HJ, Lin SP, Lee NC, Hwu WL, Lin JL, Hung PY, Niu DM. Cheng KH, et al. Among authors: lin jl, lin hy, lin sp. J Chin Med Assoc. 2010 Jun;73(6):314-8. doi: 10.1016/S1726-4901(10)70067-8. J Chin Med Assoc. 2010. PMID: 20603089 Free article.

8

High-resolution melting analysis is a more effective approach for screening TSC genes mutations.

Tsai TS, Huang MY, Chang YT, Wang CY, Lin JL, Hung PC, Lin SP, Sun CF, Wang WS, Chang CM, Chang SC, Chu DC. Tsai TS, et al. Among authors: lin jl, lin sp. Genet Test Mol Biomarkers. 2011 Jun;15(6):415-21. doi: 10.1089/gtmb.2010.0133. Epub 2011 Apr 21. Genet Test Mol Biomarkers. 2011. PMID: 21510812

9

Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA.

Lin HY, Chuang CK, Chen MR, Chiu PC, Ke YY, Niu DM, Tsai FJ, Hwu WL, Lin JL, Lin SP. Lin HY, et al. Among authors: lin jl, lin sp. Orphanet J Rare Dis. 2014 Feb 10;9:21. doi: 10.1186/1750-1172-9-21. Orphanet J Rare Dis. 2014. PMID: 24513086 Free PMC article.

10

A Truncating De Novo Point Mutation in a Young Infant with Severe Menkes Disease.

Lin YJ, Ho CS, Hsu CH, Lin JL, Chuang CK, Tsai JD, Chiu NC, Lin HY, Lin SP. Lin YJ, et al. Among authors: lin jl, lin hy, lin sp. Pediatr Neonatol. 2017 Feb;58(1):89-92. doi: 10.1016/j.pedneo.2014.05.008. Epub 2014 Nov 14. Pediatr Neonatol. 2017. PMID: 25771438 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,137 results

Search Page