B. Christensen

发表

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.

Fetal Gender and Several Cytokines Are Associated with the Number of Fetal Cells in Maternal Blood – An Observational Study

N. Uldbjerg, D. Hougaard, S. Kolvraa, 2014, PloS one.

Comparative genomic hybridization in clinical cytogenetics.

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

Characterization of Fetal Cells from the Maternal Circulation by Microarray Gene Expression Analysis - Could the Extravillous Trophoblasts Be a Target for Future Cell-Based Non-Invasive Prenatal Diagnosis?

N. Uldbjerg, B. Huppertz, Rune Hoff Lauridsen, 2013, Fetal Diagnosis and Therapy.

Epsilon Haemoglobin Specific Antibodies with Applications in Noninvasive Prenatal Diagnosis

U. Jensen, S. Kolvraa, P. Kristensen, 2009, Journal of biomedicine & biotechnology.

Microselection – affinity selecting antibodies against a single rare cell in a heterogeneous population

S. Kolvraa, P. Kristensen, I. Agerholm, 2010, Journal of cellular and molecular medicine.

Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.

A. Motulsky, W. Raskind, A. L. Jørgensen, 1992, American journal of human genetics.

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 .

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.

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.

Identification of circulating fetal cell markers by microarray analysis

N. Uldbjerg, S. Kolvraa, L. Hatt, 2012, Prenatal diagnosis.

Chorionic villus culture for prenatal diagnosis of chromosome defects: Reduction of the long‐term cultivation time

B. Christensen, S. Smidt‐Jensen, A. Lind, 1989, Prenatal diagnosis.

The Number of Endovascular Trophoblasts in Maternal Blood Increases Overnight and after Physical Activity: An Experimental Study

N. Uldbjerg, S. Kolvraa, L. Hatt, 2015, Fetal Diagnosis and Therapy.

A new marker set that identifies fetal cells in maternal circulation with high specificity

N. Uldbjerg, Rune Hoff Lauridsen, S. Kolvraa, 2014, Prenatal diagnosis.

Studies on the Isolation and Identification of Fetal Nucleated Red Blood Cells in the Circulation of Pregnant Women before and after Chorion Villus Sampling

T. Lörch, J. Philip, S. Kolvraa, 2003, Fetal Diagnosis and Therapy.

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.

Sensitivity and Specificity of the Identification of Fetal Cells in Maternal Blood by Combined Staining with Antibodies against Beta-, Gamma- and Epsilon-Globin Chains

J. Philip, S. Kolvraa, B. Christensen, 2003, Fetal Diagnosis and Therapy.

Comparative GenomicHybridization inClinical Cytogenetics

M. Kirchhoff, B. Christensen, 1995 .

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 .

Genetic amniocentesis at 7–14 weeks of gestation

J. Philip, B. Christensen, A. Lind, 1992, Prenatal diagnosis.

The Fetal Erythroblast Is Not the Optimal Target for Non-invasive Prenatal Diagnosis: Preliminary Results

J. Philip, S. Kolvraa, B. Christensen, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Early and rapid prenatal exclusion of Down's syndrome

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

ζ-, ε-, and γ-Globin mRNA in Blood Samples and CD71+ Cell Fractions from Fetuses and from Pregnant and Nonpregnant Women, with Special Attention to Identification of Fetal Erythroblasts

J. Philip, S. Sørensen, T. Hviid, 2001 .

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

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

Fetal Cells in Maternal Blood: A Comparison of Methods for Cell Isolation and Identification

T. Lörch, J. Philip, S. Kolvraa, 2005, Fetal Diagnosis and Therapy.

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.