Chen SJ - Search Results

1

Multiple congenital anomalies in association with supernumerary chromosome 47 inherited from a maternal balanced translocation.

Su PH, Chen JY, Hung HM, Chen JP, Wang CM, Chen SJ. Su PH, et al. Among authors: chen jy, chen jp, chen sj. J Formos Med Assoc. 2002 Apr;101(4):301-3. J Formos Med Assoc. 2002. PMID: 12101870

2

Interstitial deletion of chromosome 14q in a Taiwanese infant with microcephaly.

Su PH, Chen SJ, Lee IC, Wang KL, Chen JY, Hung HM, Lee CF. Su PH, et al. Among authors: chen jy, chen sj. J Formos Med Assoc. 2004 May;103(5):385-7. J Formos Med Assoc. 2004. PMID: 15216407

3

Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation.

Su PH, Chen JY, Chen SJ, Hung HM. Su PH, et al. Among authors: chen jy, chen sj. J Formos Med Assoc. 2004 Nov;103(11):853-7. J Formos Med Assoc. 2004. PMID: 15549153

4

Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation.

Su PH, Kuo PL, Chen SJ, Huang SC, Chen JY, Hung HM. Su PH, et al. Among authors: chen jy, chen sj. J Formos Med Assoc. 2005 Jul;104(7):525-30. J Formos Med Assoc. 2005. PMID: 16091833

5

Anterior mediastinal immature teratoma with precocious puberty in a child with Klinefelter syndrome.

Su PH, Luh SP, Yieh DM, Chen JY, Chen SJ, Hung HM, Liao PF. Su PH, et al. Among authors: chen jy, chen sj. J Formos Med Assoc. 2005 Aug;104(8):601-4. J Formos Med Assoc. 2005. PMID: 16193184

6

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: chen jy, chen sj. 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.

7

Clinical manifestations of chromosome 21 interstitial deletion: report of four cases.

Su PH, Chen JY, Chen SJ, Lin LL. Su PH, et al. Among authors: chen jy, chen sj. Acta Paediatr Taiwan. 2006 Nov-Dec;47(6):303-8. Acta Paediatr Taiwan. 2006. PMID: 17407982

8

Trisomy 18 with multiple rare malformations: report of one case.

Su PH, Chen JY, Hsu CH, Chen SJ, Chan SW, Lin LL. Su PH, et al. Among authors: chen jy, chen sj. Acta Paediatr Taiwan. 2007 Sep-Oct;48(5):272-5. Acta Paediatr Taiwan. 2007. PMID: 18254577

9

Trisomy 18 syndrome with incomplete Cantrell syndrome.

Hou YJ, Chen FL, Ng YY, Hu JM, Chen SJ, Chen JY, Su PH. Hou YJ, et al. Among authors: chen jy, chen fl, chen sj. Pediatr Neonatol. 2008 Jun;49(3):84-7. doi: 10.1016/S1875-9572(08)60018-2. Pediatr Neonatol. 2008. PMID: 18947004 Free article.

10

Terminal deletion of chromosome 6q.

Su PH, Chen JY, Chen SJ, Yang KC. Su PH, et al. Among authors: chen jy, chen sj. Pediatr Neonatol. 2008 Jun;49(3):88-93. doi: 10.1016/S1875-9572(08)60019-4. Pediatr Neonatol. 2008. PMID: 18947005 Free article.

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