Trifonov V - Search Results

1

Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).

Starke H, Senger G, Kossakiewicz M, Tittelbach H, Rau D, Rubtsov N, Trifonov V, Heller A, Hartmann I, Claussen U, Liehr T. Starke H, et al. Among authors: trifonov v. Prenat Diagn. 2001 Dec;21(12):1049-52. doi: 10.1002/pd.192. Prenat Diagn. 2001. PMID: 11746162

2

Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia.

Starke H, Raida M, Trifonov V, Clement JH, Loncarevic IF, Heller A, Bleck C, Nietzel A, Rubtsov N, Claussen U, Liehr T. Starke H, et al. Among authors: trifonov v. Br J Haematol. 2001 May;113(2):435-8. doi: 10.1046/j.1365-2141.2001.02787.x. Br J Haematol. 2001. PMID: 11380412 Free article.

3

Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB).

Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Rocchi M, Claussen U, Liehr T. Mrasek K, et al. Among authors: trifonov v. Cytogenet Cell Genet. 2001;93(3-4):242-8. doi: 10.1159/000056991. Cytogenet Cell Genet. 2001. PMID: 11528119

4

Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.

Dufke A, Walczak C, Liehr T, Starke H, Trifonov V, Rubtsov N, Schöning M, Enders H, Eggermann T. Dufke A, et al. Among authors: trifonov v. Eur J Hum Genet. 2001 Aug;9(8):572-6. doi: 10.1038/sj.ejhg.5200673. Eur J Hum Genet. 2001. PMID: 11528501

5

Microdissection based high resolution multicolor banding for all 24 human chromosomes.

Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, Claussen U. Liehr T, et al. Among authors: trifonov v. Int J Mol Med. 2002 Apr;9(4):335-9. Int J Mol Med. 2002. PMID: 11891523

6

First case of trisomy 13 plus mosaic trisomy 1q.

Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U. Liehr T, et al. Among authors: trifonov v. Fetal Diagn Ther. 2002 May-Jun;17(3):133-6. doi: 10.1159/000048025. Fetal Diagn Ther. 2002. PMID: 11914563

7

A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding.

Heller A, Starke H, Trifonov V, Rubtsov N, Wedding U, Loncarevic I, Bleck C, Claussen U, Liehr T. Heller A, et al. Among authors: trifonov v. Int J Oncol. 2002 Jun;20(6):1179-81. Int J Oncol. 2002. PMID: 12011996

8

Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.

Trifonov V, Seidel J, Starke H, Martina P, Beensen V, Ziegler M, Hartmann I, Heller A, Nietzel A, Claussen U, Liehr T. Trifonov V, et al. Prenat Diagn. 2003 May;23(5):427-30. doi: 10.1002/pd.595. Prenat Diagn. 2003. PMID: 12749042 No abstract available.

9

Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.

Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Claussen U, Liehr T. Mrasek K, et al. Among authors: trifonov v. Int J Mol Med. 2003 Aug;12(2):139-46. Int J Mol Med. 2003. PMID: 12851708

10

First postnatal case of mosaic del(22)/r(22).

Starke H, Mitulla B, Beensen V, Trifonov V, Rubtsov N, Heller A, Ziegler M, Neumann A, Claussen U, Liehr T. Starke H, et al. Among authors: trifonov v. Prenat Diagn. 2003 Sep;23(9):765-7. doi: 10.1002/pd.666. Prenat Diagn. 2003. PMID: 12975792 No abstract available.

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