Lin SJ - Search Results

1

Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan.

Chow JC, Chen DJ, Lin CN, Chiu CY, Huang CB, Chiu PC, Lin CH, Lin SJ, Tzeng CC. Chow JC, et al. Among authors: lin ch, lin sj, lin cn. J Formos Med Assoc. 2003 Jan;102(1):12-6. J Formos Med Assoc. 2003. PMID: 12684606

2

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.

Tzeng CC, Tsai LP, Hwu WL, Lin SJ, Chao MC, Jong YJ, Chu SY, Chao WC, Lu CL. Tzeng CC, et al. Among authors: lin sj. Am J Med Genet A. 2005 Feb 15;133A(1):37-43. doi: 10.1002/ajmg.a.30528. Am J Med Genet A. 2005. PMID: 15637705

3

Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan.

Tzeng CC, Tzeng PY, Sun HS, Chen RM, Lin SJ. Tzeng CC, et al. Among authors: lin sj. Diagn Mol Pathol. 2000 Jun;9(2):75-80. doi: 10.1097/00019606-200006000-00002. Diagn Mol Pathol. 2000. PMID: 10850542

4

An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome.

Tzeng CC, Lin SJ, Chen YJ, Kuo PL, Jong YJ, Tsai LP, Chen RM. Tzeng CC, et al. Among authors: lin sj. Diagn Mol Pathol. 2001 Mar;10(1):34-40. doi: 10.1097/00019606-200103000-00006. Diagn Mol Pathol. 2001. PMID: 11277393

5

Detection of Y-chromosome sequences in patients with X-chromosome abnormalities.

Kuo PL, Wu RC, Lin SJ, Tzeng CC, Liu HS, Huang KE. Kuo PL, et al. Among authors: lin sj. J Formos Med Assoc. 1995 Sep;94(9):529-34. J Formos Med Assoc. 1995. PMID: 8696166

6

Genetic Evaluation of Children with Global Developmental Delay--Current Status of Network Systems in Taiwan.

Foo YL, Chow JC, Lai MC, Tsai WH, Tung LC, Kuo MC, Lin SJ. Foo YL, et al. Among authors: lin sj. Pediatr Neonatol. 2015 Aug;56(4):213-9. doi: 10.1016/j.pedneo.2014.08.001. Epub 2014 Nov 4. Pediatr Neonatol. 2015. PMID: 25454079 Free article. Review.

7

X chromosome mosaicism in patients with recurrent abortion or premature ovarian failure.

Wu RC, Kuo PL, Lin SJ, Liu CH, Tzeng CC. Wu RC, et al. Among authors: lin sj. J Formos Med Assoc. 1993 Nov;92(11):953-6. J Formos Med Assoc. 1993. PMID: 7910065

8

Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan.

Su PH, Hwu WL, Chiang SC, Chiu PC, Lin SJ, Shu SG, Wang TR. Su PH, et al. Among authors: lin sj. J Formos Med Assoc. 1998 Mar;97(3):186-90. J Formos Med Assoc. 1998. PMID: 9549269

9

Detection of Y-chromosomal DNA with marker chromosomes in Turner's syndrome.

Kuo PL, Wu RC, Tzeng CC, Lin SJ, Liu SS, Huang KE. Kuo PL, et al. Among authors: lin sj. J Formos Med Assoc. 1995 Aug;94(8):474-80. J Formos Med Assoc. 1995. PMID: 7549576

10

Cytogenetic surveillance of mentally-retarded school children in southern Taiwan.

Shiue CN, Lin YH, Kuan LC, Lii LM, Tsai WH, Chen YJ, Lin SJ, Kuo PL. Shiue CN, et al. Among authors: lin sj, lin yh. J Formos Med Assoc. 2004 Mar;103(3):218-24. J Formos Med Assoc. 2004. PMID: 15124050

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