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- Prenatal diagnosis in twenty-seven pregnancies at risk for Fanconi anemia.Am. J. Hum. Genet. 1984; 36: 184S
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- Fetal diagnosis of trisomy 21 in the first trimester of pregnancy.Lancet. 1983; 1: 586
- Mechanisms by which amniotic fluid alpha-fetoprotein may be increased in fetal abnormalities.Lancet. 1976; 2: 345
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- European collaborative study in prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures.Prenat. Diagn. 1984; 4: 145-162
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- Chromosomes of mouse embryos and newborn young: Preparations from membranes and tail tips.Stain Technol. 1972; 47: 229-234
- Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative European study on 52,965 amniocenteses.Prenat. Diagn. 1984; 4: 5-44
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- Prenatal exclusion of ataxiatelangiectasia.in: Bridges B.A. Harnden D.G. Ataxia telangiectasia—a cellular and molecular link between cancer neuropathology, and immune deficiency. Wiley, New York1982: 393-400
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- Prenatal sex determination by fluorescent staining of the cervical smear for the presence of a Y chromosome: An evaluation.Am. J. Obstet. Gynecol. 1973; 115: 866
- Prenatal diagnosis of sickle cell anemia in the first trimester of pregnancy.N. Engl. J. Med. 1983; 309: 831-833
- Direct vision chorion biopsy and chromosome specific DNA probes for determination of fetal sex in first trimester prenatal diagnosis.Lancet. 1982; 2: 1416-1419
- Prenatal Tay-Sachs diagnosis by chorionic villi sampling.Lancet. 1983; 2: 286-287
- First-trimester diagnosis on chorionicvilli obtained by direct vision technique.Hum. Genet. 1984; 65: 373-376
- Data from an alpha-fetoprotein pilot screening program in Maine.Obstet. Gynecol. 1983; 62: 556-560
- Possibility of culturing foetal cells at early stages of pregnancy.Clin. Genet. 1972; 3: 286-293
- Chromosome studies in induced abortions.Clin. Genet. 1973; 4: 328-332
- Early prenatal diagnosis: A study of biopsy techniques and cell culturing from extraembryonic membranes.Clin. Genet. 1974; 6: 294-306
- Antenatal foetal diagnosis in the embryo by means of biopsy from extraembryonic membranes.Bull. Eur. Soc. Hum. Genet. 1968; 2: 23-29
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- Prenatal diagnosis of xeroderma pigmentosum (group C) using assays and unscheduled DNA synthesis and postreplication repair.Clin. Genet. 1979; 16: 137-146
- Stage II ultrasound examination for the diagnosis of fetal abnormalities with an elevated amniotic fluid alpha-fetoprotein concentration.Am. J. Obstet. Gynecol. 1982; 142: 1026-1029
- Paternal age and Down’s syndrome genotypes diagnosed prenatally: No association in New York State data.Hum. Genet. 1982; 62: 167-174
- Estimated rates of Down syndrome in live births by one year maternal age intervals for mothers aged 20–39 in a New York State study: Implications of the risk figures for genetic counseling and cost-benefit analysis of prenatal diagnosis programs.Birth Defects. 1977; XII: 124-141
- United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis.Prenat. Diagn. 1984; 4: 97-130
Jackson, L.: Chorionic Villus Newsletter 1985 (personal communication).
- Fragile X chromosome prenatal diagnosis.Am. J. Hum. Genet. 1982; 34: 130A
- Late prenatal diagnosis of fetal trisomy 18 associated with severe intrauterine growth retardation.Johns Hopkins Med. J. 1982; 151: 242-245
- Chorion biopsy in early pregnancy: A method of early prenatal diagnosis for inherited disorders.Prenat. Diagn. 1982; 2: 39-45
- Fetal chromosome analysis after transcervical placental biopsies during early pregnancy.Acta Obstet. Gynecol. Scand. 1969; 52: 355-359
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- Feasibility of first trimester prenatal diagnosis of Hunter syndrome.Lancet. 1983; 2: 1147
- Prenatal diagnosis of an unbalanced chromosome translocation identified by direct karyotyping of chorionic biopsy.Lancet. 1983; 2: 1426-1427
- Prenatal serum alpha-fetoprotein screening for neural tube defect.Obstet. Gynecol. 1982; 59: 633-639
- An association between low maternal serum alpha-fetoprotein and fetal chromosomal abnormalities.Am. J. Obstet. Gynecol. 1984; 148: 886-894
- Results and benefits of a maternal serum alpha-fetoprotein screening program.J.A.M.A. 1984; 252: 1438-1442
- Prenatal diagnosis of open neural tube defects using amniotic fluid acetylcholinesterase assay.Obstet. Gynecol. 1982; 59: 1-5
- Foetal genetic diagnosis: Development of techniques for early sampling of foetal cells.Acta Pathol. Microbiol. Scand. 1968; 73: 73-77
- Antenatal detection of hereditary disorders.Pediatrics. 1968; 42: 912-918
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- First-trimester fetal diagnosis of haemoglobinopathies: Three cases.Lancet. 1982; 2: 1414-1416
- Prenatal Tay-Sachs diagnosis by chorionic villi sampling.Lancet. 1983; 2: 286-287
- A new approach to prenatal diagnosis using trophoblast cells in maternal blood. In Bergsma, D. (ed.): New Chromosomal and Malformation Syndromes. Miami: Symposia Specialists for the National Foundation March of Dimes.Birth Defects. 1975; 11: 295
- Prenatal diagnosis of xeroderma pigmentosum: Report of the first successful case.Lancet. 1974; 2: 1109-1112
- Alpha-fetoprotein during childhood.in: Weitzel H.K. Schneider J. Alpha-Fetoprotein in Clinical Medicine. Georg Thieme, Stuttgart1979: 152-157
- First trimester chromosome analysis of complex structural rearrangements with RHA banding on chorionic villi.Lancet. 1983; 2: 1426
- High cesarean section rate in trisomy 18 births: A potential indication for late prenatal diagnosis.Am. J. Obstet. Gynecol. 1981; 140: 367-370
- Rates of trisomies 21, 18, 13 and other chromosome abnormalities in about 20,000 prenatal studies compared with estimated rates in live births.Hum. Genet. 1982; 61: 318-324
- Amniocentesis: technique and complications.in: Emery A.E.H. Antenatal Diagnosis of Genetic Disease. Churchill Livingstone, London1973
- Fetal lymphocytes in the maternal blood.Blood. 1972; 39: 153-163
- Tests appropriate for the prenatal diagnosis of ataxia telangiectasia.Prenat. Diagn. 1985; 5: 9-14
- Alpha fetoprotein in maternal serum: A new marker for detection of fetal distress and intrauterine death.Am. J. Obstet. Gynecol. 1973; 115: 48-52
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- The fragile X syndrome: Experience with prenatal diagnosis.Am. J. Hum. Genet. 1984; 36: 96S
- Use of the Y chromosome in prenatal sex determination.Nature (Lond.). 1971; 230: 52-53
- Efficient direct chromosome analyses and enzyme determination from chorionic villi samples in the first trimester of pregnancy.Hum. Genet. 1983; 63: 349-357
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- Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration: A European collaborative study on prenatal diagnoses 1981.Prenat. Diagn. 1984; 4: 81-95
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- Studies of the human trophoblast in tissue culture.Am. J. Obstet. Gynecol. 1960; 79: 636-647
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- Second report of the UK Collaborative Study on alpha-fetoprotein in relation to neural-tube defects: Amniotic fluid alpha-fetoprotein measurement in antenatal diagnosis of anencephaly and open spina bifida in early pregnancy.Lancet. 1979; 2: 651-662
- Prenatal diagnosis of Fanconi anemia.Clin. Genet. 1981; 20: 185-190
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- De novo structural rearrangements: Implications for prenatal diagnosis.in: Willey A.M. Carter J.P. Kelly S. Problems in Diagnosis and Counselling. Academic Press, New York1982: 63-75
- Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis.Prenat. Diagn. 1984; 4: 69-80
- A method of chorionic villus sampling in the first trimester of pregnancy under real time ultrasound guidance.Br. Med. J. 1983; 286: 1542-1544
- Assessment of fetal condition and amniotic fluid analysis.in: Henry J.B. Todd-Sanford-Davidsohn Clinical Diagnosis and Management by Laboratory Methods. Edition 17. W. B. Saunders Co., Philadelphia1983: 502-517
- Direct gene analysis of chorionic villi: A possible technique for first trimester antenatal diagnosis of haemoglobinopathies.Lancet. 1981; 2: 1125-1127
- A Canadian collaborative study of mosaicism in amniotic fluid cell cultures.Prenat. Diagn. 1984; 4: 131-144