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Didascalia

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H)  Diagnosi 16
1 Alpman A, Bora E, Karaca E, Cankaya T, Onay H, Cogulu O et al. Detection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease. Genet.Couns. 2004;15:99-100. No abstract available.
2 Devlin L,.Morrison PJ. Accuracy of the clinical diagnosis of Down syndrome. ULSTER.MED.J 73:4- 12.
3 DeVore GR,.Romero R. Genetic sonography: a cost-effective method for evaluating women 35 years and older who decline genetic amniocentesis. Journal of Ultrasound in Medicine 2002;21(1):5-13.
4 DeVore GR,.Romero R. Genetic sonography: an option for women of advanced maternal age with negative triple-marker maternal serum screening results. J.Ultrasound.Med 2003;22:1191-9.
5 DeVore GR. The role of fetal echocardiography in genetic sonography. Semin.Perinatol 2003;27:160-72.
6 Drummond CL, Gomes DM, Senat MV, Audibert F, Dorion A, Ville Y. Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population. Prenat.Diagn. 2003;23:1068-72.
7 Goumy C, Bonnet Dupeyron MN, Cherasse Y, Laurichesse H, Jaffray JY, Lacroute G et al. Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis. Prenat.Diagn. 2004; 24:249-56.
8 Greene N,.Platt LD. In response to 'Certificate of competence in performing specific procedures or tests in screening practice'. Prenat.Diagn. 2004;24:315. No abstract available.
9 Homer J, Bhatt S, Huang B, Thangavelu M. Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH). Prenat.Diagn. 2003;23:566-71.
10 Hsieh LJ, Hsieh TC, Yeh GP, Lin M, I, Chen M, Wang BT. Prenatal diagnosis of a fetus affected with down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping. Fetal.Diagn.Ther 19:356-60.
11 Hulten MA, Dhanjal S, Pertl B. Rapid and simple prenatal diagnosis of common chromosome disorders: Advantages and disadvantages of the molecular methods FISH and QF-PCR. REPRODUCTION 126:279-97.
12 Lee MH, Ryu HM, Kim DJ, Lee BY, Cho EH, Yang JH et al. Rapid prenatal diagnosis of Down Syndrome using quantitative fluorescent PCR in uncultured amniocytes. J.Korean.Med.Sci 2004;19:341-4.
13 Netto CB, Siqueira IR, Fochesatto C, Portela LV, Purificacao Tavares M, Souza DO et al. S100B content and SOD activity in amniotic fluid of pregnancies with Down syndrome. Clin.Biochem. 2004;37:134-7.
14 Stewart TL. Screening for aneuploidy: the genetic sonogram. Obstet.Gynecol.Clin.North.Am 2004;31:21-33.
15 Wang S, Jia C, Ren G, Ma Y, Lu W, Ding F et al. Molecular diagnosis of Down's syndrome. CHIN.MED.J 116:1773-5.
16 Yeo L,.Vintzileos AM. The use of genetic sonography to reduce the need for amniocentesis in women at high-risk for Down syndrome. Semin.Perinatol 2003;27:152-9. 
Last Edit: 29/11/2010 10:53am
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