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Sollen die Indikationen für nichtinvasive Pränataltests erweitert werden?

Gynäkologe (Berlin), 2018, Vol.51 (1), p.24-31

2018

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Pränataldiagnostik: Aktuelle medizinische Aspekte

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2013-12, Vol.56 (12), p.1662-1669

2013

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Prenatal diagnostics: current medical aspects

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2013-12, Vol.56 (12), p.1662-1669

2013

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Suspicious Prenasal Skin Thickness-to-Nasal Bone Length Ratio: Prevalence and Correlation with Other Markers in Second and Third Trimester Fetuses with Down Syndrome

Ultraschall in der Medizin, 2015-10, Vol.36 (5), p.501-506

2015

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Early preclinical development of PQR309, a novel balanced dual PI3K/mTOR inhibitor for treatment of various cancer types

Toxicology letters, 2015-10, Vol.238 (2), p.S337-S338

2015

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Prevalence of Vitamin D Deficiency Among LVAD Patients

The Journal of heart and lung transplantation, 2014-04, Vol.33 (4), p.S208-S208

2014

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Enzymatic Digestion of Adult Human Articular Cartilage Yields a Small Fraction of the Total Available Cells

Connective tissue research, 2003, Vol.44 (3-4), p.173-180

2003

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The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age

Ultraschall in der Medizin, 2011-06, Vol.32 (3), p.302-306

2011

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Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics

Cytogenetic and genome research, 2006-08, Vol.114 (3-4), p.296-301

2006

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10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

Cytogenetic and genome research, 2009-01, Vol.124 (1), p.102-105

2009

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A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset

Prenatal diagnosis, 2010-11, Vol.30 (11), p.1100-1106

2010

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First-Trimester Prenatal Diagnosis of Okihiro Syndrome

Fetal diagnosis and therapy, 2010-01, Vol.27 (4), p.222-226

2010

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Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines

International journal of radiation biology, 1999, Vol.75 (5), p.583-591

ANTOCCIA, M. STUMM, K. SAAR, R. RICORDY, P. MARASCHIO, C. TANZARELLA, A.

1999

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High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

Cytogenetic and genome research, 2001-01, Vol.92 (3-4), p.186-191

2001

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Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytes

Cytogenetic and genome research, 2003-01, Vol.103 (1-2), p.47-53

2003

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Enabling autonomic behavior in systems software with hot swapping

IBM systems journal, 2003, Vol.42 (1), p.60-76

2003

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Reducing the harmful effects of last-level cache polluters with an OS-level, software-only pollute buffer

2008 41st IEEE/ACM International Symposium on Microarchitecture, 2008, p.258-269

2008

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Algorithms implementing distributed shared memory

Computer (Long Beach, Calif.), 1990-05, Vol.23 (5), p.54-64

1990

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Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14

Cytogenetic and genome research, 2005-01, Vol.108 (4), p.283-286

2005

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Improved definition of chromosomal breakpoints using high-resolution multicolour banding

Human genetics, 2001-06, Vol.108 (6), p.478-483

2001

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Extracorporeal Membrane Oxygenation and Cardiopulmonary Bypass in Pediatric Drowning Patients

The Thoracic and cardiovascular surgeon, 2017, Vol.65 (S 01), p.S1-S110

2017

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Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification

Human genetics, 2003-12, Vol.114 (1), p.51-67

2003

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Hybrid Approach for Branch Pulmonary Artery Stenosis in Congenital Heart Disease

The Thoracic and cardiovascular surgeon, 2018, Vol.66 (S 01), p.S1-S110

2018

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Impact of Delayed Sternal Closure on Wound Infections following Paediatric Cardiac Surgery

The Thoracic and cardiovascular surgeon, 2018, Vol.66 (S 01), p.S1-S110

2018

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Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics

Cytogenetic and genome research, 2001-01, Vol.93 (3-4), p.188-194

2001

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Sollen die Indikationen für nichtinvasive Pränataltests erweitert werden?

Pränataldiagnostik: Aktuelle medizinische Aspekte

Prenatal diagnostics: current medical aspects

Suspicious Prenasal Skin Thickness-to-Nasal Bone Length Ratio: Prevalence and Correlation with Other Markers in Second and Third Trimester Fetuses with Down Syndrome

Early preclinical development of PQR309, a novel balanced dual PI3K/mTOR inhibitor for treatment of various cancer types

Prevalence of Vitamin D Deficiency Among LVAD Patients

Enzymatic Digestion of Adult Human Articular Cartilage Yields a Small Fraction of the Total Available Cells

The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age

Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset

First-Trimester Prenatal Diagnosis of Okihiro Syndrome

Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines

High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytes

Enabling autonomic behavior in systems software with hot swapping

Reducing the harmful effects of last-level cache polluters with an OS-level, software-only pollute buffer

Algorithms implementing distributed shared memory

Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14

Improved definition of chromosomal breakpoints using high-resolution multicolour banding

Extracorporeal Membrane Oxygenation and Cardiopulmonary Bypass in Pediatric Drowning Patients

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification

Hybrid Approach for Branch Pulmonary Artery Stenosis in Congenital Heart Disease

Impact of Delayed Sternal Closure on Wound Infections following Paediatric Cardiac Surgery

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics

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