Hsieh FJ - Search Results

1

Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.

Hwa HL, Ko TM, Chang YY, Huang CH, Su YN, Tseng LH, Hsieh FJ. Hwa HL, et al. Among authors: hsieh fj. Prenat Diagn. 2004 Feb;24(2):121-4. doi: 10.1002/pd.817. Prenat Diagn. 2004. PMID: 14974120

2

Rapid prenatal diagnosis of X-linked chronic granulomatous disease using a denaturing high-performance liquid chromatography (DHPLC) system.

Chien SC, Lee CN, Hung CC, Tsao PN, Su YN, Hsieh FJ. Chien SC, et al. Among authors: hsieh fj. Prenat Diagn. 2003 Dec 30;23(13):1092-6. doi: 10.1002/pd.761. Prenat Diagn. 2003. PMID: 14691999

3

Prenatal cytogenetic diagnosis in amniocentesis.

Hsieh FJ, Ko TM, Tseng LH, Chang LS, Pan MF, Chuang SM, Lee TY, Chen HY. Hsieh FJ, et al. J Formos Med Assoc. 1992 Mar;91(3):276-82. J Formos Med Assoc. 1992. PMID: 1354688

4

DNA polymorphism and globin chain analysis in the prenatal diagnosis of beta-thalassaemia major in Taiwan.

Ko TM, Hsieh FJ, Lee TY. Ko TM, et al. Among authors: hsieh fj. Prenat Diagn. 1990 Apr;10(4):237-44. doi: 10.1002/pd.1970100405. Prenat Diagn. 1990. PMID: 1973294

5

Prenatal diagnosis of Chinese homozygous alpha-thalassaemia 1 and haemoglobin H disease by analysis of alpha- and phi zeta-globin genes in chorionic villi and amniocytes.

Ko TM, Hsieh FJ, Hsu PM, Lee TY. Ko TM, et al. Among authors: hsieh fj. Prenat Diagn. 1989 Oct;9(10):715-25. doi: 10.1002/pd.1970091007. Prenat Diagn. 1989. PMID: 2594699

6

Prenatal diagnosis of X-linked hydrocephalus in a Chinese family with four successive affected pregnancies.

Ko TM, Hwa HL, Tseng LH, Hsieh FJ, Huang SF, Lee TY. Ko TM, et al. Among authors: hsieh fj. Prenat Diagn. 1994 Jan;14(1):57-60. doi: 10.1002/pd.1970140110. Prenat Diagn. 1994. PMID: 7910398

7

Prenatal diagnosis of Hb H disease due to compound heterozygosity for South-east Asian deletion and Hb constant spring by polymerase chain reaction.

Ko TM, Tseng LH, Hsieh FJ, Lee TY. Ko TM, et al. Among authors: hsieh fj. Prenat Diagn. 1993 Feb;13(2):143-6. doi: 10.1002/pd.1970130210. Prenat Diagn. 1993. PMID: 8464834

8

Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: report of a case.

Chung YP, Hwa HL, Tseng LH, Shyu MK, Lee CN, Shih JC, Hsieh FJ. Chung YP, et al. Among authors: hsieh fj. Prenat Diagn. 1998 Jan;18(1):73-7. doi: 10.1002/(sici)1097-0223(199801)18:1<73::aid-pd215>3.0.co;2-8. Prenat Diagn. 1998. PMID: 9483644

9

Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome.

Shaw SW, Chen CP, Cheng PJ, Wang TH, Hou JW, Lin CT, Chang SD, Hwa HL, Lin JL, Chao AS, Soong YK, Hsieh FJ. Shaw SW, et al. Among authors: hsieh fj. J Hum Genet. 2008;53(2):136-143. doi: 10.1007/s10038-007-0229-z. Epub 2007 Dec 12. J Hum Genet. 2008. PMID: 18074101

10

Cost-effectiveness analysis of triple test in second-trimester maternal serum screening for Down's syndrome: an experience from Taiwan with decreasing birth rate but increasing population of old pregnant women.

Hwa HL, Yen MF, Lin CL, Ko TM, Hsieh FJ, Chen TH. Hwa HL, et al. Among authors: hsieh fj. J Eval Clin Pract. 2008 Apr;14(2):191-7. doi: 10.1111/j.1365-2753.2007.00831.x. Epub 2008 Feb 18. J Eval Clin Pract. 2008. PMID: 18284525

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