Stumm M - Search Results

1

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

Stumm M, Neubauer S, Keindorff S, Wegner RD, Wieacker P, Sauer R. Stumm M, et al. Cytogenet Cell Genet. 2001;92(3-4):186-91. doi: 10.1159/000056900. Cytogenet Cell Genet. 2001. PMID: 11435685

2

No evidence for deletions of the NBS1 gene in lymphomas.

Stumm M, von Ruskowsky A, Siebert R, Harder S, Varon R, Wieacker P, Schlegelberger B. Stumm M, et al. Cancer Genet Cytogenet. 2001 Apr 1;126(1):60-2. doi: 10.1016/s0165-4608(00)00390-3. Cancer Genet Cytogenet. 2001. PMID: 11343781

3

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

Tönnies H, Stumm M, Wegner RD, Chudoba I, Kalscheuer V, Neitzel H. Tönnies H, et al. Among authors: stumm m. Cytogenet Cell Genet. 2001;93(3-4):188-94. doi: 10.1159/000056983. Cytogenet Cell Genet. 2001. PMID: 11528111

4

Radiosensitivity of ataxia telangiectasia and Nijmegen breakage syndrome homozygotes and heterozygotes as determined by three-color FISH chromosome painting.

Neubauer S, Arutyunyan R, Stumm M, Dörk T, Bendix R, Bremer M, Varon R, Sauer R, Gebhart E. Neubauer S, et al. Among authors: stumm m. Radiat Res. 2002 Mar;157(3):312-21. doi: 10.1667/0033-7587(2002)157[0312:roatan]2.0.co;2. Radiat Res. 2002. PMID: 11839094

5

Retrospective diagnosis and subsequent prenatal diagnosis of Nijmegen breakage syndrome.

Muschke P, Gola H, Varon R, Röpke A, Zumkeller W, Wieacker P, Stumm M. Muschke P, et al. Among authors: stumm m. Prenat Diagn. 2004 Feb;24(2):111-3. doi: 10.1002/pd.803. Prenat Diagn. 2004. PMID: 14974117

6

Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.

Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M. Zumkeller W, et al. Among authors: stumm m. Am J Med Genet A. 2004 Sep 1;129A(3):261-4. doi: 10.1002/ajmg.a.30125. Am J Med Genet A. 2004. PMID: 15326625

7

Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.

Wegner RD, Schröck E, Obladen M, Becker R, Stumm M, Sperling K. Wegner RD, et al. Among authors: stumm m. Prenat Diagn. 1996 Aug;16(8):741-8. doi: 10.1002/(SICI)1097-0223(199608)16:8<741::AID-PD931>3.0.CO;2-W. Prenat Diagn. 1996. PMID: 8878285

8

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

Saar K, Chrzanowska KH, Stumm M, Jung M, Nürnberg G, Wienker TF, Seemanová E, Wegner RD, Reis A, Sperling K. Saar K, et al. Among authors: stumm m. Am J Hum Genet. 1997 Mar;60(3):605-10. Am J Hum Genet. 1997. PMID: 9042920 Free PMC article.

9

Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patient.

Chrzanowska K, Stumm M, Bialecka M, Saar K, Bernatowska-Matuszkiewicz E, Michalkiewicz J, Barszcz S, Reis A, Wegner RD. Chrzanowska K, et al. Among authors: stumm m. Clin Genet. 1997 May;51(5):309-13. doi: 10.1111/j.1399-0004.1997.tb02479.x. Clin Genet. 1997. PMID: 9212178

10

Female pseudohermaphroditism caused by caudal dysgenesis.

Wieacker P, Grumpelt U, Schulz T, Gharavi B, Avenarius S, Jakubiczka S, Stumm M. Wieacker P, et al. Among authors: stumm m. Cytogenet Cell Genet. 2000;91(1-4):296-9. doi: 10.1159/000056860. Cytogenet Cell Genet. 2000. PMID: 11173872 Review.

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