The 7th international conference on early prenatal diagnosis: Some personal impressions

[1]  P. Malet,et al.  Assessment of polyploidy in human morulae and blastocysts using co-culture and fluorescent in-situ hybridization. , 1993, Human reproduction.

[2]  I. Wilkins,et al.  Prenatal diagnosis of Dandy‐Walker malformation in a family displaying X‐linked inheritance , 1993, Prenatal diagnosis.

[3]  J. Wiley,et al.  Confined placental mosaicism, IUGR, and adverse pregnancy outcome: A controlled retrospective U.K. collaborative survey , 1994, Prenatal diagnosis.

[4]  E. Pergament,et al.  Fertilization and early embryology: Sexual differentiation and preimplantation cell growth , 1994 .

[5]  J. Philip,et al.  Fluorescence in situ hybridization with a chromosome 21‐specific cosmid contig: 1‐day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells , 1994, Prenatal diagnosis.

[6]  J. Mandelbaum,et al.  Chromosome investigations in early life. II. Human preimplantation embryos. , 1987, Human reproduction.

[7]  A. Handyside.  Biopsy of Human Cleavage Stage Embryos and Sexing by DNA Amplification , 1991 .

[8]  J. Harper,et al.  Identification of the sex of human preimplantation embryos in two hours using an improved spreading method and fluorescent in-situ hybridization (FISH) using directly labelled probes. , 1994, Human reproduction.

[9]  J. Grudzinskas,et al.  Serum PAPP‐A and free β‐hCG are first‐trimester screening markers for down syndrome , 1994 .

[10]  J. Simpson,et al.  Isolating fetal cells from maternal blood. Advances in prenatal diagnosis through molecular technology. , 1993, JAMA.

[11]  W. Schmid,et al.  Ultrasound screening for chromosomal anomalies in the first trimester of pregnancy , 1993, Prenatal diagnosis.

[12]  Z. Rosenwaks,et al.  Diagnosis of major chromosome aneuploidies in human preimplantation embryos. , 1993, Human reproduction.

[13]  J. Harper,et al.  The current status of preimplantation diagnosis , 1994 .

[14]  J. Harper,et al.  Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos , 1995, Prenatal diagnosis.

[15]  P. Devroey,et al.  Polymerase chain reaction analysis of the cystic fibrosis ΔF508 mutation in human blastomeres following oocyte injection of a single sperm from a carrier , 1993, Prenatal diagnosis.

[16]  D. Griffin,et al.  Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH). , 1993, Human molecular genetics.

[17]  N. Wald,et al.  Four‐marker serum screening for Down's syndrome , 1994, Prenatal diagnosis.

[18]  K. Spencer,et al.  First‐trimester free beta (hCG) screening for Down syndrome , 1993, Prenatal diagnosis.

[19]  N. Carter,et al.  Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five‐colour fluorescence in situ hybridization , 1994, Prenatal diagnosis.

[20]  D. Griffin,et al.  Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation. , 1993, BMJ.

[21]  L. Shulman,et al.  Significance of septations in isolated fetal cystic hygroma detected in the first trimester , 1994, Prenatal diagnosis.

[22]  E. Engel,et al.  Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection. , 1991, American journal of medical genetics.

[23]  C. Rodeck,et al.  Y chromosome sequence DNA amplified from peripheral blood of women in early pregnancy , 1994, The Lancet.

[24]  R. Hubert,et al.  Whole genome amplification from a single cell: implications for genetic analysis. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[25]  C. J. Asperen,et al.  Cytogenetic findings in 1250 chorionic villus samples obtained in the first trimester with clinical follow‐up of the first 1000 pregnancies , 1989, British journal of obstetrics and gynaecology.

[26]  S. Goodburn,et al.  Second‐trimester maternal serum screening using alpha‐fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: Experience of a regional programme , 1994, Prenatal diagnosis.

[27]  K. Nicolaides,et al.  Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy. , 1992, BMJ.

[28]  Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis. , 1992 .

[29]  C. Strom,et al.  Preconception and preimplantation diagnosis for cystic fibrosis , 1992, Prenatal diagnosis.

[30]  Z. Rosenwaks,et al.  Sex determination of human embryos using the polymerase chain reaction and confirmation by fluorescence in situ hybridization , 1994, Fertility and sterility.