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Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements

Prenatal diagnosis, 2003-08, Vol.23 (8), p.652-662

2003

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Cystic fibrosis: selecting the prenatal screening strategy of choice

Prenatal diagnosis, 2003-06, Vol.23 (6), p.474-483

2003

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The time of appearance and disappearance of fetal DNA from the maternal circulation

Prenatal diagnosis, 1995-07, Vol.15 (7), p.641-646

1995

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Relative efficiency of FISH on metaphase and interphase nuclei from non-mosaic trisomic or triploid fibroblast cultures

Prenatal diagnosis, 2000-02, Vol.20 (2), p.159-162

2000

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Increased nuchal translucency as a prenatal manifestation of congenital adrenal hyperplasia

Prenatal diagnosis, 2001-04, Vol.21 (4), p.314-316

2001

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FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryos

Prenatal diagnosis, 2000-07, Vol.20 (7), p.552-560

2000

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Women's choices for fetal chromosome analysis

Prenatal diagnosis, 1991-01, Vol.11 (1), p.23-28

1991

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The fetal intrahepatic umbilical vein as an alternative to cord needling for prenatal diagnosis and therapy

Prenatal diagnosis, 1988-11, Vol.8 (9), p.665-671

1988

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Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family

Prenatal diagnosis, 1995-07, Vol.15 (7), p.647-654

1995

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Further predictors of renal dysplasia in fetal obstructive uropathy: Bladder pressure and biochemistry of 'fresh' urine

Prenatal diagnosis, 1991-03, Vol.11 (3), p.159-166

1991

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Testosterone levels in midtrimester maternal and fetal plasma and amniotic fluid

Prenatal diagnosis, 1985-05, Vol.5 (3), p.175-181

1985

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Intrauterine manometry: Technique and application to fetal pathology

Prenatal diagnosis, 1989-04, Vol.9 (4), p.243-254

1989

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Prenatal detection of rubella-specific IgM in fetal sera

Prenatal diagnosis, 1985-01, Vol.5 (1), p.21-26

1985

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Extraction of DNA from amniotic fluid cells for the early prenatal diagnosis of genetic disease

Prenatal diagnosis, 1991-01, Vol.11 (1), p.41-46

1991

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Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid

Prenatal diagnosis, 1987-03, Vol.7 (3), p.203-214

1987

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Neonatal alloimmune thrombocytopenia due to anti-P1A1 (anti-hpa-1a): Importance of paternal and fetal platelet typing for assessment of fetal risk

Prenatal diagnosis, 1992-11, Vol.12 (11), p.955-958

1992

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Normal blood cell values in the early mid-trimester fetus

Prenatal diagnosis, 1985-11, Vol.5 (6), p.367-373

1985

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Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy

Prenatal diagnosis, 2005-12, Vol.25 (12), p.1111-1116

2005

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Prenatal diagnosis of mandibulofacial dysostosis

Prenatal diagnosis, 1984-05, Vol.4 (3), p.201-205

1984

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Multiple sulphatase deficiency: Prenatal diagnosis using chorionic villi

Prenatal diagnosis, 1988-05, Vol.8 (4), p.303-306

1988

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Invasive diagnostic procedures in twin pregnancies

Prenatal diagnosis, 2005-09, Vol.25 (9), p.751-758

2005

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First trimester diagnosis of adenosine deaminase deficiency

Prenatal diagnosis, 1987-10, Vol.7 (8), p.561-565

1987

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Selective feticide of the affected twin by fetoscopic air embolism

Prenatal diagnosis, 1982-07, Vol.2 (3), p.189-194

1982

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Fetal cystic hygromata: Insights gained from fetal blood sampling

Prenatal diagnosis, 1990-03, Vol.10 (3), p.189-193

1990

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Immunoreactive trypsin level in fetoscopically-obtained cord sera of second trimester fetuses

Prenatal diagnosis, 1984-07, Vol.4 (4), p.303-306

1984

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Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements

Cystic fibrosis: selecting the prenatal screening strategy of choice

The time of appearance and disappearance of fetal DNA from the maternal circulation

Relative efficiency of FISH on metaphase and interphase nuclei from non-mosaic trisomic or triploid fibroblast cultures

Increased nuchal translucency as a prenatal manifestation of congenital adrenal hyperplasia

FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryos

Women's choices for fetal chromosome analysis

The fetal intrahepatic umbilical vein as an alternative to cord needling for prenatal diagnosis and therapy

Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family

Further predictors of renal dysplasia in fetal obstructive uropathy: Bladder pressure and biochemistry of 'fresh' urine

Testosterone levels in midtrimester maternal and fetal plasma and amniotic fluid

Intrauterine manometry: Technique and application to fetal pathology

Prenatal detection of rubella-specific IgM in fetal sera

Extraction of DNA from amniotic fluid cells for the early prenatal diagnosis of genetic disease

Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid

Neonatal alloimmune thrombocytopenia due to anti-P1A1 (anti-hpa-1a): Importance of paternal and fetal platelet typing for assessment of fetal risk

Normal blood cell values in the early mid-trimester fetus

Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy

Prenatal diagnosis of mandibulofacial dysostosis

Multiple sulphatase deficiency: Prenatal diagnosis using chorionic villi

Invasive diagnostic procedures in twin pregnancies

First trimester diagnosis of adenosine deaminase deficiency

Selective feticide of the affected twin by fetoscopic air embolism

Fetal cystic hygromata: Insights gained from fetal blood sampling

Immunoreactive trypsin level in fetoscopically-obtained cord sera of second trimester fetuses

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