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T Bryndorf

Showing results (1-10 of 21) with videos related to

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Prenatal Diagnosis|December 1, 1994
Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH)J Philip, T Bryndorf, B Christensen
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|April 1, 1995
[Rapid detection of numerical aberrations of chromosomes in the first trimester of pregnancy by using fluorescence in situ hybridization (FISH)]Y Xiang, T Bryndorf, J Philip, et al.
Fetal Diagnosis and Therapy|March 1, 1994
Prenatal diagnosis by fluorescence in situ hybridization on chorionic villus cells: nonsignificance of maternal cell contaminationT Bryndorf, B Christensen, Y Xiang, et al.
Prenatal Diagnosis|April 1, 1992
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridizationB Christensen, T Bryndorf, J Philip, et al.
Prenatal Diagnosis|September 1, 1993
Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cellsT Bryndorf, B Christensen, Y Xiang, et al.
Acta Obstetricia Et Gynecologica Scandinavica|January 26, 2000
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 samplesT Bryndorf, C Lundsteen, A Lamb, et al.
Prenatal Diagnosis|July 1, 1993
Prenatal diagnosis by in situ hybridization on uncultured amniocytes: reduced sensitivity and potential risk of misdiagnosis in blood-stained samplesB Christensen, T Bryndorf, J Philip, et al.
Prenatal Diagnosis|April 1, 1997
Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trialT Bryndorf, B Christensen, M Vad, et al.
Clinical Genetics|April 12, 2001
Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISHL N Schultz, P Schmidt, A Tabor, et al.
Prenatal Diagnosis|February 1, 1994
Fluorescence in situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cellsT Bryndorf, B Christensen, Y Xiang, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|December 1, 1994
Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH)J Philip, T Bryndorf, B Christensen
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|April 1, 1995
[Rapid detection of numerical aberrations of chromosomes in the first trimester of pregnancy by using fluorescence in situ hybridization (FISH)]Y Xiang, T Bryndorf, J Philip, et al.
Fetal Diagnosis and Therapy|March 1, 1994
Prenatal diagnosis by fluorescence in situ hybridization on chorionic villus cells: nonsignificance of maternal cell contaminationT Bryndorf, B Christensen, Y Xiang, et al.
Prenatal Diagnosis|April 1, 1992
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridizationB Christensen, T Bryndorf, J Philip, et al.
Prenatal Diagnosis|September 1, 1993
Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cellsT Bryndorf, B Christensen, Y Xiang, et al.
Acta Obstetricia Et Gynecologica Scandinavica|January 26, 2000
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 samplesT Bryndorf, C Lundsteen, A Lamb, et al.
Prenatal Diagnosis|July 1, 1993
Prenatal diagnosis by in situ hybridization on uncultured amniocytes: reduced sensitivity and potential risk of misdiagnosis in blood-stained samplesB Christensen, T Bryndorf, J Philip, et al.
Prenatal Diagnosis|April 1, 1997
Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trialT Bryndorf, B Christensen, M Vad, et al.
Clinical Genetics|April 12, 2001
Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISHL N Schultz, P Schmidt, A Tabor, et al.
Prenatal Diagnosis|February 1, 1994
Fluorescence in situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cellsT Bryndorf, B Christensen, Y Xiang, et al.
Pageof 3