Yu JS - Search Results

1

Leptin expression and leptin receptor gene polymorphisms in growth hormone deficiency patients.

Su PH, Chen JY, Yu JS, Chen SJ, Yang SF. Su PH, et al. Among authors: yu js. Hum Genet. 2011 Apr;129(4):455-62. doi: 10.1007/s00439-010-0941-1. Epub 2011 Jan 5. Hum Genet. 2011. PMID: 21207066

2

De Novo incontinentia pigmenti in female twins.

Su PH, Chen JY, Yu JS, Su CM, Huang TC, Chen SJ. Su PH, et al. Among authors: yu js. Acta Paediatr Taiwan. 2004 May-Jun;45(3):178-80. Acta Paediatr Taiwan. 2004. PMID: 15493740

3

Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.

Su PH, Chen JY, Chen SJ, Yu JS. Su PH, et al. Among authors: yu js. J Formos Med Assoc. 2006 Jun;105(6):518-21. doi: 10.1016/S0929-6646(09)60194-7. J Formos Med Assoc. 2006. PMID: 16801042 Free article.

4

Mutations and new polymorphic changes in the TCOF1 gene of patients with oculo-auriculo-vertebral spectrum and Treacher-Collins syndrome.

Su PH, Yu JS, Chen JY, Chen SJ, Li SY, Chen HN. Su PH, et al. Among authors: yu js. Clin Dysmorphol. 2007 Oct;16(4):261-7. doi: 10.1097/MCD.0b013e3281c108d2. Clin Dysmorphol. 2007. PMID: 17786119

5

Benign familial neonatal convulsions: novel mutation in a newborn.

Lee IC, Chen JY, Chen YJ, Yu JS, Su PH. Lee IC, et al. Among authors: yu js. Pediatr Neurol. 2009 May;40(5):387-91. doi: 10.1016/j.pediatrneurol.2008.12.004. Pediatr Neurol. 2009. PMID: 19380078

6

Kabuki make-up (Niikawa-Kuroki) syndrome with mosaicism ring chromosome X and incomplete XIST gene expression.

Su PH, Kuo PL, Chen SJ, Chen JY, Yu JS, Liu YL, Kao IW. Su PH, et al. Among authors: yu js. Acta Paediatr Taiwan. 2007 Jan-Feb;48(1):28-31. Acta Paediatr Taiwan. 2007. PMID: 19653414

7

Persistent falcine sinus and unilateral renal agenesis in a girl with Sotos syndrome.

Su PH, Yu JS, Chen SJ, Chen JY, Tsao TF. Su PH, et al. Among authors: yu js. Clin Dysmorphol. 2011 Jan;20(1):42-46. doi: 10.1097/MCD.0b013e32833ff281. Clin Dysmorphol. 2011. PMID: 21084978

8

Interstitial deletions of the short arm of chromosome 4 in a patient with mental retardation and focal seizure.

Su PH, Lee IC, Chen JY, Chen SJ, Yu JS, Tsao TF. Su PH, et al. Among authors: yu js. Pediatr Neonatol. 2011 Jun;52(3):165-8. doi: 10.1016/j.pedneo.2011.03.009. Epub 2011 Apr 12. Pediatr Neonatol. 2011. PMID: 21703560 Free article.

9

Study of the leptin levels and its gene polymorphisms in patients with idiopathic short stature and growth hormone deficiency.

Su PH, Yang SF, Yu JS, Chen SJ, Chen JY. Su PH, et al. Among authors: yu js. Endocrine. 2012 Aug;42(1):196-204. doi: 10.1007/s12020-012-9632-0. Epub 2012 Feb 19. Endocrine. 2012. PMID: 22350661

10

Study of leptin levels and gene polymorphisms in patients with central precocious puberty.

Su PH, Yang SF, Yu JS, Chen SJ, Chen JY. Su PH, et al. Among authors: yu js. Pediatr Res. 2012 Apr;71(4 Pt 1):361-7. doi: 10.1038/pr.2011.69. Epub 2012 Feb 15. Pediatr Res. 2012. PMID: 22391636

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