M. Stumm

发表

Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation.

Dagmar Wieczorek, Roberto Giorda, Marcella Zollino, 2002, American journal of human genetics.

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

K. Schütze, R. Schneider-Stock, J. Ryś, 2002, The Journal of pathology.

G2‐phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome

A. di Masi, A. Antoccia, C. Tanzarella, 2002, Cell proliferation.

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

A. Antoccia, C. Tanzarella, K. Saar, 1999, International journal of radiation biology.

Analysis of BRCA 1 and BRCA 2 Mutations in Hungarian Families with Breast or Breast-Ovarian Cancer

R. Wegner, K. Sperling, M. Stumm, 2006 .

A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia.

P. Wieacker, M. Stumm, K. Jentsch‐Ullrich, 2000, Cancer genetics and cytogenetics.

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

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

R. Wegner, P. Wieacker, M. Stumm, 2001, Cytogenetic and Genome Research.

Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies

P. Wieacker, H. Tönnies, M. Stumm, 1999, European Journal of Pediatrics.

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

P. Wieacker, M. Stumm, J. Kleinstein, 2003, Cytogenetic and Genome Research.

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

P. Wieacker, M. Volleth, M. Stumm, 2004, Cytogenetic and Genome Research.

Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons.

R. Wegner, K. Sperling, M. Stumm, 1997, American journal of human genetics.

P-190. FISH analysis of unfertilized human oocytes using locus-specific DNA probes

P. Wieacker, M. Stumm, J. Kleinstein, 1999 .

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

M. Volleth, H. Tönnies, L. Neumann, 2001, Journal of medical genetics.

The presynaptic cytomatrix protein Bassoon: sequence and chromosomal localization of the human BSN gene.

C. Garner, T. Boeckers, J. Bockmann, 1999, Genomics.

Partial trisomy 9p12p21.3 with a normal phenotype

P. Wieacker, M. Volleth, I. Chudoba, 2002, Journal of medical genetics.

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

T. Wienker, E. Seemanová, R. Wegner, 1997, American journal of human genetics.

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

R. Wegner, I. Chudoba, H. Tönnies, 2001, Cytogenetic and Genome Research.

The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1.

E. Seemanová, R. Wegner, K. Chrzanowska, 1995, American journal of human genetics.

No evidence for deletions of the NBS1 gene in lymphomas.

R. Siebert, P. Wieacker, B. Schlegelberger, 2001, Cancer genetics and cytogenetics.

Preferential Inactivation of a dupX(q23 → q27–28) Chromosome in a Girl with Mental Retardation and Dysmorphy

V. Kalscheuer, P. Wieacker, M. Volleth, 2001, Human Heredity.

High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements

P. Wieacker, M. Stumm, A. Pelz, 2002, Annals of Hematology.

Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma.

P. Wieacker, H. Tönnies, M. Stumm, 1999, Cancer genetics and cytogenetics.