T. Bryndorf

发表

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

Ryan L. Collins, A. Silahtaroglu, N. Tommerup, 2018, American journal of human genetics.

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

J. Philip, T. Bryndorf, B. Christensen, 1993, Prenatal diagnosis.

Comparative genomic hybridization in clinical cytogenetics.

C. Lundsteen, T. Gerdes, J. Philip, 1995, American journal of human genetics.

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

M. Kirchhoff, T. Bryndorf, A. Bisgaard, 2006, American journal of medical genetics. Part A.

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.

T. Gerdes, M. Kirchhoff, T. Bryndorf, 2007, European journal of medical genetics.

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

M. Kirchhoff, T. Bryndorf, A. Bisgaard, 2007, Clinical dysmorphology.

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.

J. Bogstad, A. Pinborg, M. Toftager, 2018, Fertility and sterility.

Cumulative live birth rates after one ART cycle including all subsequent frozen–thaw cycles in 1050 women: secondary outcome of an RCT comparing GnRH-antagonist and GnRH-agonist protocols

J. Bogstad, A. Pinborg, M. Toftager, 2017, Human reproduction.

Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation

V. Kalscheuer, C. Menzel, R. Ullmann, 2006, Cytogenetic and Genome Research.

Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (Fish)

J. Philip, T. Bryndorf, J Philip, 1994, Prenatal diagnosis.

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

J. Philip, T. Bryndorf, B. Christensen, 1993, Prenatal diagnosis.

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

J. Philip, T. Bryndorf, B. Christensen, 1993, BMJ.

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

J. Philip, T. Bryndorf, B. Christensen, 1992 .

Risk of severe ovarian hyperstimulation syndrome in GnRH antagonist versus GnRH agonist protocol: RCT including 1050 first IVF/ICSI cycles.

J. Bogstad, A. Pinborg, M. Toftager, 2016, Human reproduction.

The most common chromosome aberration detected by high-resolution comparative genomic hybridization in vulvar intraepithelial neoplasia is not seen in vulvar squamous cell carcinoma

C. Lundsteen, M. Kirchhoff, T. Bryndorf, 2004, Cytogenetic and Genome Research.

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

J. Philip, T. Bryndorf, B. Christensen, 1994, Prenatal diagnosis.

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

K. Klinger, J. Philip, B. Ward, 1996, American journal of human genetics.

Image analysis in comparative genomic hybridization.

P. Lichter, C. Lundsteen, T. Gerdes, 1995, Cytometry.

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

C. Lundsteen, T. Gerdes, J. Philip, 1999, Genes, chromosomes & cancer.

4q35 deletion and 10p15 duplication associated with immunodeficiency

Z. Tümer, N. Tommerup, H. Ropers, 2006, American journal of medical genetics. Part A.

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

Z. Tümer, N. Tommerup, M. Kirchhoff, 2006, American journal of medical genetics. Part A.

Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial.

J. Philip, J. Parner, T. Bryndorf, 1997, Prenatal diagnosis.

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

J. Philip, J. Parner, T. Bryndorf, 1997 .

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

Tommy Gerdes, T. Gerdes, M. Kirchhoff, 2005, American journal of medical genetics. Part A.

Early and rapid prenatal exclusion of Down's syndrome

J. Philip, T. Bryndorf, K. Sundberg, 1994, The Lancet.

Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISH

C. Lundsteen, T. Bryndorf, B. Christensen, 2001, Clinical genetics.

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

Tommy Gerdes, T. Gerdes, M. Kirchhoff, 2005, Electrophoresis.

Mental distress and personality in women undergoing GnRH agonist versus GnRH antagonist protocols for assisted reproductive technology.

J. Bogstad, A. Pinborg, K. Holst, 2015, Human reproduction.

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.

J. Bogstad, A. Pinborg, M. Toftager, 2019, Reproductive biomedicine online.

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.

C. Lundsteen, T. Gerdes, J. Maahr, 1999, Genes, chromosomes & cancer.

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

C. Lundsteen, J. Philip, T. Bryndorf, 1992, Prenatal diagnosis.

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.

C. Lundsteen, T. Gerdes, J. Maahr, 1999 .

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

T. Bryndorf, A. Andersen, A. K. Jensen, 2023, Reproductive sciences.

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

C. Lundsteen, J. Philip, T. Bryndorf, 2000, Acta obstetricia et gynecologica Scandinavica.