Mkrtchyan H - Search Results

1

Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.

Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise A, Mkrtchyan H. Polityko AD, et al. Among authors: mkrtchyan h. Eur J Med Genet. 2009 Jul-Aug;52(4):207-10. doi: 10.1016/j.ejmg.2009.03.016. Epub 2009 Apr 16. Eur J Med Genet. 2009. PMID: 19375526

2

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.

Weise A, Gross M, Mrasek K, Mkrtchyan H, Horsthemke B, Jonsrud C, Von Eggeling F, Hinreiner S, Witthuhn V, Claussen U, Liehr T. Weise A, et al. Among authors: mkrtchyan h. Int J Mol Med. 2008 Feb;21(2):189-200. doi: 10.3892/ijmm.21.2.189. Int J Mol Med. 2008. PMID: 18204785

3

Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics.

Manvelyan M, Kempf P, Weise A, Mrasek K, Heller A, Lier A, Höffken K, Fricke HJ, Sayer HG, Liehr T, Mkrtchyan H. Manvelyan M, et al. Among authors: mkrtchyan h. Int J Mol Med. 2009 Sep;24(3):335-41. doi: 10.3892/ijmm_00000237. Int J Mol Med. 2009. PMID: 19639225

4

Early embryonic chromosome instability results in stable mosaic pattern in human tissues.

Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Volleth M, Weise A. Mkrtchyan H, et al. PLoS One. 2010 Mar 9;5(3):e9591. doi: 10.1371/journal.pone.0009591. PLoS One. 2010. PMID: 20231887 Free PMC article.

5

Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band).

Liehr T, Weise A, Hinreiner S, Mkrtchyan H, Mrasek K, Kosyakova N. Liehr T, et al. Among authors: mkrtchyan h. Methods Mol Biol. 2010;659:231-8. doi: 10.1007/978-1-60761-789-1_16. Methods Mol Biol. 2010. PMID: 20809315

6

Heteromorphic variants of chromosome 9.

Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, Schreyer I, Nelle H, Stumm M, Wegner RD, Reising-Ackermann G, Merkas M, Brecevic L, Martin T, Rodríguez L, Bhatt S, Ziegler M, Kreskowski K, Weise A, Sazci A, Vorsanova S, Cioffi Mde B, Ergul E. Kosyakova N, et al. Among authors: mkrtchyan h. Mol Cytogenet. 2013 Apr 1;6(1):14. doi: 10.1186/1755-8166-6-14. Mol Cytogenet. 2013. PMID: 23547710 Free PMC article.

7

POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism.

Weise A, Gross M, Hinreiner S, Witthuhn V, Mkrtchyan H, Liehr T. Weise A, et al. Among authors: mkrtchyan h. Methods Mol Biol. 2010;659:291-8. doi: 10.1007/978-1-60761-789-1_22. Methods Mol Biol. 2010. PMID: 20809321

8

The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?

Karaer K, Ergun MA, Weise A, Ewers E, Liehr T, Kosyakova N, Mkrtchyan H. Karaer K, et al. Among authors: mkrtchyan h. Genet Couns. 2010;21(4):397-404. Genet Couns. 2010. PMID: 21290969

9

Murine multicolor banding.

Kosyakova N, Trifonov V, Romanenko S, Mkrtchyan H, Graphodatsky A, Liehr T. Kosyakova N, et al. Among authors: mkrtchyan h. Tsitologiia. 2013;55(4):259-60. Tsitologiia. 2013. PMID: 23875460 Review.

10

A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.

Fickelscher I, Starke H, Schulze E, Ernst G, Kosyakova N, Mkrtchyan H, MacDermont K, Sebire N, Liehr T. Fickelscher I, et al. Among authors: mkrtchyan h. Prenat Diagn. 2007 Aug;27(8):783-5. doi: 10.1002/pd.1776. Prenat Diagn. 2007. PMID: 17546703

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