Speicher MR - Search Results

1

Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).

Holinski-Feder E, Reyniers E, Uhrig S, Golla A, Wauters J, Kroisel P, Bossuyt P, Rost I, Jedele K, Zierler H, Schwab S, Wildenauer D, Speicher MR, Willems PJ, Meitinger T, Kooy RF. Holinski-Feder E, et al. Among authors: speicher mr. Am J Hum Genet. 2000 Jan;66(1):16-25. doi: 10.1086/302703. Am J Hum Genet. 2000. PMID: 10631133 Free PMC article.

2

Karyotyping human chromosomes by combinatorial multi-fluor FISH.

Speicher MR, Gwyn Ballard S, Ward DC. Speicher MR, et al. Nat Genet. 1996 Apr;12(4):368-75. doi: 10.1038/ng0496-368. Nat Genet. 1996. PMID: 8630489

3

An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH).

Eils R, Uhrig S, Saracoglu K, Sätzler K, Bolzer A, Petersen I, Chassery J, Ganser M, Speicher MR. Eils R, et al. Among authors: speicher mr. Cytogenet Cell Genet. 1998;82(3-4):160-71. doi: 10.1159/000015092. Cytogenet Cell Genet. 1998. PMID: 9858809

4

Multiplex-FISH for pre- and postnatal diagnostic applications.

Uhrig S, Schuffenhauer S, Fauth C, Wirtz A, Daumer-Haas C, Apacik C, Cohen M, Müller-Navia J, Cremer T, Murken J, Speicher MR. Uhrig S, et al. Among authors: speicher mr. Am J Hum Genet. 1999 Aug;65(2):448-62. doi: 10.1086/302508. Am J Hum Genet. 1999. PMID: 10417288 Free PMC article.

5

An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH.

Azofeifa J, Fauth C, Kraus J, Maierhofer C, Langer S, Bolzer A, Reichman J, Schuffenhauer S, Speicher MR. Azofeifa J, et al. Among authors: speicher mr. Am J Hum Genet. 2000 May;66(5):1684-8. doi: 10.1086/302875. Epub 2000 Apr 4. Am J Hum Genet. 2000. PMID: 10762552 Free PMC article.

6

Breakpoint within the nucleolus organizer region resulting in a reciprocal translocation t (4;14)(q21;p12).

Grabowski M, Fauth C, Wirtz A, Speicher MR. Grabowski M, et al. Among authors: speicher mr. Am J Med Genet. 2000 Jun 5;92(4):264-8. Am J Med Genet. 2000. PMID: 10842293

7

Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding.

Speicher MR, Petersen S, Uhrig S, Jentsch I, Fauth C, Eils R, Petersen I. Speicher MR, et al. Lab Invest. 2000 Jul;80(7):1031-41. doi: 10.1038/labinvest.3780108. Lab Invest. 2000. PMID: 10908148 Free article.

8

Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry.

Schmidt H, Uhrig S, Lederer G, Murken J, Speicher MR, Schuffenhauer S. Schmidt H, et al. Among authors: speicher mr. J Med Genet. 2000 Oct;37(10):804-7. doi: 10.1136/jmg.37.10.804. J Med Genet. 2000. PMID: 11183189 Free PMC article. No abstract available.

9

Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL).

Brown J, Saracoglu K, Uhrig S, Speicher MR, Eils R, Kearney L. Brown J, et al. Among authors: speicher mr. Nat Med. 2001 Apr;7(4):497-501. doi: 10.1038/86581. Nat Med. 2001. PMID: 11283680 No abstract available.

10

New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization.

Saracoglu K, Brown J, Kearney L, Uhrig S, Azofeifa J, Fauth C, Speicher MR, Eils R. Saracoglu K, et al. Among authors: speicher mr. Cytometry. 2001 May 1;44(1):7-15. doi: 10.1002/1097-0320(20010501)44:1<7::aid-cyto1076>3.0.co;2-g. Cytometry. 2001. PMID: 11309803 Free article.

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