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Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes

American journal of human genetics, 2018-06, Vol.102 (6), p.1090-1103

2018

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A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers

Reproductive sciences (Thousand Oaks, Calif.), 2023-12, Vol.30 (12), p.3597-3609

2023

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Quality of life and psychosocial and physical well-being among 1,023 women during their first assisted reproductive technology treatment: secondary outcome to a randomized controlled trial comparing gonadotropin-releasing hormone (GnRH) antagonist and GnRH agonist protocols

Fertility and sterility, 2018-01, Vol.109 (1), p.154-164

2018

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Perinatal outcomes in 521 gestations after fresh and frozen cycles: a secondary outcome of a randomized controlled trial comparing GnRH antagonist versus GnRH agonist protocols

Reproductive biomedicine online, 2019-10, Vol.39 (4), p.659-664

2019

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MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions

European journal of medical genetics, 2007-01, Vol.50 (1), p.33-42

2007

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Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection)

Electrophoresis, 2005-11, Vol.26 (22), p.4327-4332

2005

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Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplication

American journal of medical genetics. Part A, 2005-12, Vol.139A (3), p.231-233

2005

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Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features

American journal of medical genetics. Part A, 2006-10, Vol.140A (20), p.2180-2187

2006

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Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma

Genes chromosomes & cancer, 1999-02, Vol.24 (2), p.144-150

1999

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Early and rapid prenatal exclusion of Down's syndrome

The Lancet (British edition), 1994-03, Vol.343 (8900), p.802-802

1994

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Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplification

American journal of medical genetics. Part A, 2005-12, Vol.139 (3), p.231-233

2005

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Twins with mental retardation and an interstitial deletion 7q34q36.2 leading to the diagnosis of long QT syndrome

American journal of medical genetics. Part A, 2006-03, Vol.140A (6), p.644-648

2006

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Comparative genomic hybridization in clinical cytogenetics

American journal of human genetics, 1995-11, Vol.57 (5), p.1211-1220

1995

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Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata

Clinical dysmorphology, 2007-04, Vol.16 (2), p.109

2007

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Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples

Acta obstetricia et gynecologica Scandinavica, 2000-01, Vol.79 (1), p.8-14

2000

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PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES BY FLUORESCENCE IN SITU HYBRIDIZATION: EXPERIENCE WITH 2000 UNCULTURED AMNIOTIC FLUID SAMPLES IN A PROSPECTIVE PRECLINICAL TRIAL

Prenatal diagnosis, 1997-04, Vol.17 (4), p.333-341

1997

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Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples

Acta obstetricia et gynecologica Scandinavica, 2000, Vol.79 (1), p.8-14

2000

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Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH

American journal of human genetics, 1996-10, Vol.59 (4), p.918-926

1996

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Development and clinical studies of in situ hybridization techniques in prenatal diagnosis

Bryndorf, Thue

1998

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Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization

Prenatal diagnosis, 1992-04, Vol.12 (4), p.241-250

1992

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Prenatal diagnosis by in situ hybridization on uncultured amniocytes: Reduced sensitivity and potential risk of misdiagnosis in blood-stained samples

Prenatal diagnosis, 1993-07, Vol.13 (7), p.581-587

1993

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Development and clinical studies of in situ hybridization techniques in prenatal diagnosis

Danish medical bulletin, 1998-06, Vol.45 (3), p.298

Bryndorf, T

1998

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Fluorescence in situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells

Prenatal diagnosis, 1994-02, Vol.14 (2), p.87-96

1994

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New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report

BMJ (Online), 1992-06, Vol.304 (6841), p.1536

1992

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Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells

Prenatal diagnosis, 1993-09, Vol.13 (9), p.815-823

1993

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Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes

A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers

Quality of life and psychosocial and physical well-being among 1,023 women during their first assisted reproductive technology treatment: secondary outcome to a randomized controlled trial comparing gonadotropin-releasing hormone (GnRH) antagonist and GnRH agonist protocols

Perinatal outcomes in 521 gestations after fresh and frozen cycles: a secondary outcome of a randomized controlled trial comparing GnRH antagonist versus GnRH agonist protocols

MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions

Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection)

Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplication

Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features

Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma

Early and rapid prenatal exclusion of Down's syndrome

Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplification

Twins with mental retardation and an interstitial deletion 7q34q36.2 leading to the diagnosis of long QT syndrome

Comparative genomic hybridization in clinical cytogenetics

Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata

Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples

PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES BY FLUORESCENCE IN SITU HYBRIDIZATION: EXPERIENCE WITH 2000 UNCULTURED AMNIOTIC FLUID SAMPLES IN A PROSPECTIVE PRECLINICAL TRIAL

Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples

Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH

Development and clinical studies of in situ hybridization techniques in prenatal diagnosis

Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization

Prenatal diagnosis by in situ hybridization on uncultured amniocytes: Reduced sensitivity and potential risk of misdiagnosis in blood-stained samples

Development and clinical studies of in situ hybridization techniques in prenatal diagnosis

Fluorescence in situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells

New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report

Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells

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