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Benefit vs potential harm of genome‐wide prenatal cfDNA testing requires further investigation and should not be dismissed based on current data

Ultrasound in obstetrics & gynecology, 2020-05, Vol.55 (5), p.695-696

2020

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Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012

Human reproduction update, 2013-07, Vol.19 (4), p.318-329

2013

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P14.03: Prenatal diagnosis and counselling of Leri‐Weill dyschondrosteosis

Ultrasound in obstetrics & gynecology, 2015-09, Vol.46 (S1), p.165-165

2015

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Congenital hydrocephalus in clinical practice: A genetic diagnostic approach

European journal of medical genetics, 2011-11, Vol.54 (6), p.e542-e547

2011

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Identification of Subgroups of High-grade Oligodendroglial Tumors by Comparative Genomic Hybridization

Journal of neuropathology and experimental neurology, 1999-06, Vol.58 (6), p.606-612

1999

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P–381 Deciphering the genetic cause of recurrent and sporadic pregnancy loss

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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The nature and prevalence of chromosomal dynamics in early spontaneous pregnancy loss

EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, Vol.32, p.24

2024

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Genetic reflection of glioblastoma biopsy material in xenografts: characterization of 11 glioblastoma xenograft lines by comparative genomic hybridization

Journal of neurosurgery, 2000-04, Vol.92 (4), p.652

2000

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Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping

Cancer research (Chicago, Ill.), 1999, Vol.59 (1), p.141-150

1999

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P09.02: Uniparental disomy 14q32.2 in a fetus presenting with omphalocele

Ultrasound in obstetrics & gynecology, 2011-10, Vol.38 (S1), p.199-200

2011

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Saponin pre-treatment in pre-embedding electron microscopic in situ hybridization for detection of specific RNA sequences in cultured cells: a methodological study

The journal of histochemistry and cytochemistry, 1995-10, Vol.43 (10), p.1005-1018

1995

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Imaging of RNA in situ hybridization by atomic force microscopy

Journal of microscopy (Oxford), 1996-06, Vol.182 (3), p.192-199

1996

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Advanced-stage cervical carcinomas are defined by a recurrent pattern of chromosomal aberrations revealing high genetic instability and a consistent gain of chromosome arm 3q

Genes chromosomes & cancer, 1997-08, Vol.19 (4), p.233-240

1997

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Individualized choice in prenatal diagnosis: the impact of karyotyping and standalone rapid aneuploidy detection on quality of life

Prenatal diagnosis, 2010-10, Vol.30 (10), p.928-936

2010

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Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms

Genes chromosomes & cancer, 2001-04, Vol.30 (4), p.349-363

2001

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Does confined placental mosaicism account for adverse perinatal outcomes in IVF pregnancies?

Human reproduction (Oxford), 2008-05, Vol.23 (5), p.1107-1112

2008

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The impact of rapid aneuploidy detection (RAD) in addition to karyotyping versus karyotyping on maternal quality of life

Prenatal diagnosis, 2010-05, Vol.30 (5), p.425-433

2010

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AgarCyto: A Novel Cell-processing Method for Multiple Molecular Diagnostic Analyses of the Uterine Cervix

The journal of histochemistry and cytochemistry, 2000-05, Vol.48 (5), p.709-718

2000

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Session 49: Biomarkers of Early Pregnancy Outcome

Human reproduction (Oxford), 2010-06, Vol.25 (suppl-1), p.i74-i75

2010

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Novel murine B‐cell lymphoma/leukemia model to study BCL2‐driven oncogenesis

International journal of cancer, 2005-05, Vol.114 (6), p.917-925

2005

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Feasibility of Virtual Reality in Elderly with Dementia

Dementia Lab 2019. Making Design Work: Engaging with Dementia in Context, p.146-149

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Monitoring morphology and signal during non-radioactive in situ hybridization procedures by reflection-contrast microscopy and transmission electron microscopy

The journal of histochemistry and cytochemistry, 1995-07, Vol.43 (7), p.665-674

1995

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Localization by fluorescence in situ hybridization (FISH) of human mitochondrial polymerase gamma (POLG) to human chromosome band 15q24-->q26, and of mouse mitochondrial polymerase gamma (Polg) to mouse chromosome band 7E, with confirmation by direct sequence analysis of bacterial artificial chromosomes (BACs)

Cytogenetics and cell genetics, 1997, Vol.78 (3-4), p.281

1997

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Tumor cytogenetics revisited : Comparative genomic hybridization and spectral karyotyping

Journal of molecular medicine (Berlin, Germany), 1997-11, Vol.75 (11-12), p.801-814

1997

Volltextzugriff (PDF)

Detection of specific messenger RNA by electron microscopic in situ hybridization: implications for nucleocytoplasmic transport

European journal of cell biology, 1995-12, Vol.68 (4), p.470-474

1995

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Benefit vs potential harm of genome‐wide prenatal cfDNA testing requires further investigation and should not be dismissed based on current data

Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012

P14.03: Prenatal diagnosis and counselling of Leri‐Weill dyschondrosteosis

Congenital hydrocephalus in clinical practice: A genetic diagnostic approach

Identification of Subgroups of High-grade Oligodendroglial Tumors by Comparative Genomic Hybridization

P–381 Deciphering the genetic cause of recurrent and sporadic pregnancy loss

The nature and prevalence of chromosomal dynamics in early spontaneous pregnancy loss

Genetic reflection of glioblastoma biopsy material in xenografts: characterization of 11 glioblastoma xenograft lines by comparative genomic hybridization

Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping

P09.02: Uniparental disomy 14q32.2 in a fetus presenting with omphalocele

Saponin pre-treatment in pre-embedding electron microscopic in situ hybridization for detection of specific RNA sequences in cultured cells: a methodological study

Imaging of RNA in situ hybridization by atomic force microscopy

Advanced-stage cervical carcinomas are defined by a recurrent pattern of chromosomal aberrations revealing high genetic instability and a consistent gain of chromosome arm 3q

Individualized choice in prenatal diagnosis: the impact of karyotyping and standalone rapid aneuploidy detection on quality of life

Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms

Does confined placental mosaicism account for adverse perinatal outcomes in IVF pregnancies?

The impact of rapid aneuploidy detection (RAD) in addition to karyotyping versus karyotyping on maternal quality of life

AgarCyto: A Novel Cell-processing Method for Multiple Molecular Diagnostic Analyses of the Uterine Cervix

Session 49: Biomarkers of Early Pregnancy Outcome

Novel murine B‐cell lymphoma/leukemia model to study BCL2‐driven oncogenesis

Feasibility of Virtual Reality in Elderly with Dementia

Monitoring morphology and signal during non-radioactive in situ hybridization procedures by reflection-contrast microscopy and transmission electron microscopy

Tumor cytogenetics revisited : Comparative genomic hybridization and spectral karyotyping

Detection of specific messenger RNA by electron microscopic in situ hybridization: implications for nucleocytoplasmic transport

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