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Outcome of first‐trimester chorionic villus sampling for genetic investigation in multiple pregnancy

Ultrasound in obstetrics & gynecology, 2001-03, Vol.17 (3), p.209-216

2001

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Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samples

Journal of medical genetics, 1999-04, Vol.36 (4), p.300-303

1999

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Low maternal serum levels of pregnancy associated plasma protein A (PAPP‐A) in the first trimester in association with abnormal fetal karyotype

BJOG : an international journal of obstetrics and gynaecology, 1993-04, Vol.100 (4), p.324-326

1993

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First‐trimester Down's syndrome screening using nuchal translucency: a prospective study in patients undergoing chorionic villus sampling

Ultrasound in obstetrics & gynecology, 1995-01, Vol.5 (1), p.9-14

1995

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First trimester concentrations of pregnancy associated plasma protein A and placental protein 14 in Down's syndrome

BMJ, 1992-07, Vol.305 (6844), p.28-28

1992

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Chorionic villus sampling safety

American journal of obstetrics and gynecology, 1996-03, Vol.174 (3), p.807-811

1996

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RhD genotyping by quantitative fluorescent polymerase chain reaction: a new approach

BJOG : an international journal of obstetrics and gynaecology, 2000-12, Vol.107 (12), p.1498-1502

2000

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First-trimester fetal reduction to a singleton infant or twins: Outcome in relation to the final number and karyotyping before reduction by transabdominal chorionic villus sampling

American journal of obstetrics and gynecology, 2004-12, Vol.191 (6), p.2035-2040

2004

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Chorionic villus sampling and amniocentesis

Current opinion in obstetrics & gynecology, 2005-04, Vol.17 (2), p.197-201

2005

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Management of multiple pregnancy: fetal reduction and prenatal diagnosis

Reproductive biomedicine online, 2006, Vol.13, p.18-18

2006

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Serum PAPP-A and free β-hCG are first-trimester screening markers for down syndrome

Prenatal diagnosis, 1994-11, Vol.14 (11), p.1043-1047

1994

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Chorionic villus sampling

Current opinion in obstetrics & gynecology, 1995-04, Vol.7 (2), p.109-116

Brambati, B

1995

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The Euro-Team Early Pregnancy (ETEP) protocol for recurrent miscarriage

Human reproduction (Oxford), 1995-06, Vol.10 (6), p.1516-1520

1995

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Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions

Human reproduction (Oxford), 1987-11, Vol.2 (8), p.735-739

1987

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Improvement in outcomes of multifetal pregnancy reduction with increased experience

American journal of obstetrics and gynecology, 2001-01, Vol.184 (2), p.97-103

2001

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Selective termination for structural, chromosomal, and mendelian anomalies: International experience

American journal of obstetrics and gynecology, 1999-10, Vol.181 (4), p.893-897

1999

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Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

Neuromuscular disorders : NMD, 1999-05, Vol.9 (3), p.190-198

1999

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Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy

Human genetics, 1983-01, Vol.63 (4), p.349-357

1983

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Ethical guidance on human embryonic and fetal tissue transplantation: a European overview

Medicine, health care, and philosophy, 2002, Vol.5 (1), p.79-90

2002

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Prenatal diagnosis of genetic diseases: Special Issue: Millennium Issue: Historical Reviews in Obstetrics and Gynecology

European journal of obstetrics & gynecology and reproductive biology, 2000, Vol.90 (2), p.165-169

BRAMBATI, B

2000

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Prenatal diagnosis of genetic diseases

European Journal of Obstetrics and Gynecology, 2000-06, Vol.90 (2), p.165-169

Brambati, Bruno

2000

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First-trimester fetal screening of cystic fibrosis in low-risk population

The Lancet (British edition), 1993-09, Vol.342 (8871), p.624-624

1993

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Maternal age-specific rates of 47,+21 and other cytogenetic abnormalities diagnosed in the first trimester of pregnancy in chorionic villus biopsy specimens: comparison with rates expected from observations at amniocentesis

American journal of human genetics, 1988-06, Vol.42 (6), p.797-807

1988

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Transabdominal chorionic villus sampling: A freehand ultrasound- guided technique

American journal of obstetrics and gynecology, 1987-07, Vol.157 (1), p.134-137

1987

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Automated detection of rare fetal cells in maternal blood: eliminating the false-positive XY signals in XX pregnancies

American journal of obstetrics and gynecology, 2004-06, Vol.190 (6), p.1571-1578

2004

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Outcome of first‐trimester chorionic villus sampling for genetic investigation in multiple pregnancy

Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samples

Low maternal serum levels of pregnancy associated plasma protein A (PAPP‐A) in the first trimester in association with abnormal fetal karyotype

First‐trimester Down's syndrome screening using nuchal translucency: a prospective study in patients undergoing chorionic villus sampling

First trimester concentrations of pregnancy associated plasma protein A and placental protein 14 in Down's syndrome

Chorionic villus sampling safety

RhD genotyping by quantitative fluorescent polymerase chain reaction: a new approach

First-trimester fetal reduction to a singleton infant or twins: Outcome in relation to the final number and karyotyping before reduction by transabdominal chorionic villus sampling

Chorionic villus sampling and amniocentesis

Management of multiple pregnancy: fetal reduction and prenatal diagnosis

Serum PAPP-A and free β-hCG are first-trimester screening markers for down syndrome

Chorionic villus sampling

The Euro-Team Early Pregnancy (ETEP) protocol for recurrent miscarriage

Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions

Improvement in outcomes of multifetal pregnancy reduction with increased experience

Selective termination for structural, chromosomal, and mendelian anomalies: International experience

Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy

Ethical guidance on human embryonic and fetal tissue transplantation: a European overview

Prenatal diagnosis of genetic diseases: Special Issue: Millennium Issue: Historical Reviews in Obstetrics and Gynecology

Prenatal diagnosis of genetic diseases

First-trimester fetal screening of cystic fibrosis in low-risk population

Maternal age-specific rates of 47,+21 and other cytogenetic abnormalities diagnosed in the first trimester of pregnancy in chorionic villus biopsy specimens: comparison with rates expected from observations at amniocentesis

Transabdominal chorionic villus sampling: A freehand ultrasound- guided technique

Automated detection of rare fetal cells in maternal blood: eliminating the false-positive XY signals in XX pregnancies

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