Leandro Michelon; Homero Vallada. A seguir descreveremos alguns desses estudos. Results from the National Comorbidity Survey. Arch Gen Psychiatry. Soc Psychiatry Psychiatr Epidemiol. Screening for bipolar disorder in the community.
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Milunsky A. Johns Hopkins University Press. Castro I. Simpson J. Invasive procedures for prenatal diagnosis: Any future left? Serr D. Diagnosis of sex before birth using cells from amniotic fluid.
Makowski E. Detection of Sex of fetuses by the incidence of sex chromatin in nuclei of cells in amniotic fluid. Fuchs F. Possibility of antenatal examination of fetal chromosome. Steele M. Chromosome analysis of human amniotic fluid cells.
Thiede H. Antenatal analysis of the human chromosomes. Jacobson C. Intrauterine diagnosis and management of genetic defects. Brock D. Alpha-fetoprotein in the antenatal diagnosis of anencephaly and spine bifida. Woo J. A short history of the developments of ultrasound in obstetrics and gynecology. Merkatz I. An association between low maternal serum alpha-fetoprotein and fetal chromosome abnormalities. Bogart M. Abnormal maternal serum chorionic gonadotropine levels in pregnancies with fetal chromosome abnormalities, Prenat.
Wald N. Canick J. Low second trimester maternal serum unconjugated estriol in pregnancies with Down syndrome. Macintosh M.
Maternal serum human chorionic gonadotrophin and pregnancy-associated plasma protein a markers. Spencer K. Screening for trisomy 21 in twin pregnancies in the first trimester using free p-hCG and PAPP-A, combined with fetal nuchal translucency thickness. Russo M. A historical and practical review of first trimester aneuploidy screening. International Prenatal Screening Research. Haddow J. J Med. Jones K. WB Saunders. Nicolaides K. Fetal nuchal translucency: Ultrasound screening for chromosomal defects in first trimester of pregnancy.
Johnson M. First trimester simple hygroma: Cause and outcome. Snijders R. L, Nicolaides K. First-trimester ultrasound screening for chromosomal defects. Obstet Gynecol. Brambati B. Correct estimation of parameters for ultrasound nuchal translucency screening. De Biasio P. First-trimester screening for Down syndrome using nuchal translucency measurement with free beta-hCG and.
Falsos positivos. Krantz D. First trimester Down syndrome screening using dried blood biochemistry and nuchal translucency. Wapner R. Gupta G. Sheth F. Evolution of Cytogenetics in Disease Diagnosis. Bianchi D. Isolation of fetal DNA from nucleated erytrocytes in maternal blood. Isolating fetal cells in maternal circulation for prenatal diagnosis.
Mieke W. The use of in vitro expanded erythroid cells in a model system for the isolation of fetal cells from maternal blood. Silveira Ramos E. Carrera M. Wells D. Clinical utilization of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation.
Handyside A. Clinical evaluation of preimplantation genetic diagnosis. Strategies for preimplantation genetic diagnosis of single gene disorders by DNA amplification. Stern HJ. Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions.
Ulli H. Use of spectral image analysis for chromosome enumeration in polar bodies, oocytes and metaphase-stage blastomeres. Evans M. Early amniocentesis: What exactly does it mean?. Brumfield C. Pregnancy outcome following genetic amniocentesis at versus weeks gestation. Johnson J. The Early Amniocentesis Study: A randomized clinical trial of early amniocentesis versus midtrimester.
Eiben B. On the complication risk of Early Amniocentesis versus Standard Amniocentesis. Sundberg K. Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus. Comparison of Chorion Villus Sampling and Early Amniocentesis for karyotyping in singleton pregnancies. Cederholm M. A prospective comparative study on transabdominal chorionic villus sampling and amniocentesis performed at weeks gestation. Daniel A. A study of early amniocentesis for prenatal cytogenetic diagnosis.
Tharmaratnam S. Early amniocentesis: Effect of removing a reduced volume of amniotic fluid on. Nadler H. Role of amniocentesis in the intrauterine detection of genetic disorders. Carrera J. Salvat Editores. Rosas A. In: Delascio D. Elejalde B. Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: Its feasibility, risks, complications and use in early genetic prenatal diagnosis.
Herència lligada al sexe
O Diagnóstico Pré-Natal