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Two Decades of Endovascular Repair of Popliteal Artery Aneurysm—A Meta-analysis

European journal of vascular and endovascular surgery, 2015-09, Vol.50 (3), p.351-359

2015

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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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Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR

Osteoarthritis and cartilage, 2012-09, Vol.20 (9), p.1039-1045

2012

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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, 2009-04, Vol.124 (1), p.102-105

2009

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Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints

International journal of molecular medicine, 2007-06, Vol.19 (6), p.855-864

2007

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Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

Journal of medical genetics, 2002-06, Vol.39 (6), p.434-439

2002

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Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

Cell, 1998-05, Vol.93 (3), p.467-476

1998

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Frequency of CFTR gene mutations in males participating in an ICSI programme

Human reproduction (Oxford), 1999-07, Vol.14 (7), p.1833-1834

1999

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Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH

Journal of medical genetics, 2001-06, Vol.38 (6), p.e21-e21

2001

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Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation

American journal of human genetics, 2002-08, Vol.71 (2), p.276-285

2002

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Increased cancer risk of heterozygotes with NBS1 germline mutations in poland

International journal of cancer, 2004-08, Vol.111 (1), p.67-71

2004

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No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non‐Hodgkin's lymphoma of childhood and adolescence

British journal of haematology, 2000-04, Vol.109 (1), p.117-120

2000

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Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease

European journal of pediatrics, 1999-07, Vol.158 (7), p.531-536

1999

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Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

European journal of human genetics : EJHG, 2002-12, Vol.10 (12), p.790-800

2002

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Radiosensitivity of Ataxia Telangiectasia and Nijmegen Breakage Syndrome Homozygotes and Heterozygotes as Determined by Three-Color FISH Chromosome Painting

Radiation research, 2002-03, Vol.157 (3), p.312-321

2002

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Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Journal of molecular medicine (Berlin, Germany), 2000-01, Vol.78 (5), p.282-286

2000

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Expression of mRNA for ROS-generating NADPH oxidases in the aging stomach

Experimental gerontology, 2005-04, Vol.40 (4), p.353-357

2005

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In vivo angiogenesis in normal and portal hypertensive rats: role of basic fibroblast growth factor and nitric oxide

Journal of hepatology, 2001-05, Vol.34 (5), p.644-650

2001

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Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations

American journal of medical genetics, 2004-04, Vol.126A (3), p.272-277

2004

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Increased angiogenesis in portal hypertensive rats: Role of nitric oxide

Hepatology (Baltimore, Md.), 1999-04, Vol.29 (4), p.1044-1049

1999

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Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomy

The Prostate, 2004-04, Vol.59 (1), p.59-68

2004

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FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy

European journal of human genetics : EJHG, 1999-10, Vol.7 (7), p.748-756

1999

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The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

American journal of human genetics, 1997-03, Vol.60 (3), p.605-610

1997

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Significance of loss of heterozygosity of the RB1 gene during tumour progression in well-differentiated liposarcomas

The Journal of pathology, 2002-08, Vol.197 (5), p.654-660

2002

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Partial trisomy 9p12p21.3 with a normal phenotype

Journal of medical genetics, 2002-02, Vol.39 (2), p.141-144

2002

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Two Decades of Endovascular Repair of Popliteal Artery Aneurysm—A Meta-analysis

Prenatal diagnostics: current medical aspects

Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR

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

Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

Frequency of CFTR gene mutations in males participating in an ICSI programme

Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH

Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation

Increased cancer risk of heterozygotes with NBS1 germline mutations in poland

No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non‐Hodgkin's lymphoma of childhood and adolescence

Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

Radiosensitivity of Ataxia Telangiectasia and Nijmegen Breakage Syndrome Homozygotes and Heterozygotes as Determined by Three-Color FISH Chromosome Painting

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Expression of mRNA for ROS-generating NADPH oxidases in the aging stomach

In vivo angiogenesis in normal and portal hypertensive rats: role of basic fibroblast growth factor and nitric oxide

Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations

Increased angiogenesis in portal hypertensive rats: Role of nitric oxide

Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomy

FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

Significance of loss of heterozygosity of the RB1 gene during tumour progression in well-differentiated liposarcomas

Partial trisomy 9p12p21.3 with a normal phenotype

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