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Items: 1 to 20 of 146

1.

Mitotic chromosome preparations from mouse cells for karyotyping.

Akeson EC, Davisson MT.

Curr Protoc Hum Genet. 2001 May;Chapter 4:Unit4.10. doi: 10.1002/0471142905.hg0410s25.

PMID:
18428279
2.

Cytogenetic analysis by chromosome painting.

Carter NP.

Cytometry. 1994 Mar 15;18(1):2-10. Review.

3.

Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridization.

Daniely M, Barkai G, Goldman B, Aviram-Goldring A.

Cytogenet Cell Genet. 1999;86(1):51-5.

PMID:
10516433
4.

Cytogenetic analysis of cardiovascular disease: karyotyping.

Jarmuz M, Shaffer LG.

Methods Mol Med. 2006;128:1-9.

PMID:
17071985
5.

Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.

Veldman T, Vignon C, Schröck E, Rowley JD, Ried T.

Nat Genet. 1997 Apr;15(4):406-10.

PMID:
9090389
6.

Assessing the quality of donor cells: karyotyping methods.

Bonnet-Garnier A, Veillard AC, Bed'Hom B, Hayes H, Britton-Davidian J.

Methods Mol Biol. 2015;1222:83-99. doi: 10.1007/978-1-4939-1594-1_7.

PMID:
25287340
7.

The application of an in situ karyotyping technique for mesenchymal stromal cells: a validation and comparison study with classical G-banding.

Hwang SM, See CJ, Choi J, Kim SY, Choi Q, Kim JA, Kwon J, Park SN, Im K, Oh IH, Lee DS.

Exp Mol Med. 2013 Dec 20;45:e68. doi: 10.1038/emm.2013.133.

8.

Hybridization-based karyotyping of mouse chromosomes: hybridization-bands.

Liechty MC, Carpio CM, Aytay S, Clase AC, Puschus KL, Sims KR, Davis LM, Hozier JC.

Cytogenet Cell Genet. 1999;86(1):34-8.

PMID:
10516429
9.

Spectral karyotyping analysis of head and neck squamous cell carcinoma.

Singh B, Gogineni S, Goberdhan A, Sacks P, Shaha A, Shah J, Rao P.

Laryngoscope. 2001 Sep;111(9):1545-50.

PMID:
11568603
11.

Multiplex-fluorescence in situ hybridization for chromosome karyotyping.

Geigl JB, Uhrig S, Speicher MR.

Nat Protoc. 2006;1(3):1172-84.

PMID:
17406400
13.

Chromosome preparation from cultured cells.

Howe B, Umrigar A, Tsien F.

J Vis Exp. 2014 Jan 28;(83):e50203. doi: 10.3791/50203.

14.

Fluorescence in situ hybridization analysis of sex-chromosome mosaicism in azoospermic men.

Okada H, Dobashi M, Yamazaki T, Fujisawa M, Arakawa S, Kamidono S.

J Androl. 2001 Nov-Dec;22(6):970-2.

15.

Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities.

Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck J, Jalal S, Shaffer LG, Papenhausen P, Kozma C, Phelan MC, Kjeldsen E, Schonberg SA, O'Brien P, Biesecker L, du Manoir S, Ried T.

Hum Genet. 1997 Dec;101(3):255-62.

PMID:
9439652
16.

Prenatal detection of a de novo Yqh-acrocentric translocation.

Ng LK, Kwok YK, Tang LY, Ng PP, Ghosh A, Lau ET, Tang MH.

Clin Biochem. 2006 Mar;39(3):219-23. Epub 2006 Mar 3.

PMID:
16515778
17.

Spectral karyotyping study of chromosome abnormalities in human leukemia.

Zhao L, Hayes K, Khan Z, Glassman A.

Cancer Genet Cytogenet. 2001 Jun;127(2):143-7. Erratum in: Cancer Genet Cytogenet 2001 Nov;131(1):94-5.

PMID:
11425454
18.

(T2AG3)n telomeric sequence hybridization indicating centric fusion rearrangements in the karyotype of the rodent oryzomys subflavus.

Andrades-Miranda J, Zanchin NI, Oliveira LF, Langguth AR, Mattevi MS.

Genetica. 2002;114(1):11-6.

PMID:
11990754
19.

Small marker chromosome identification in metaphase and interphase using centromeric multiplex fish (CM-FISH).

Henegariu O, Bray-Ward P, Artan S, Vance GH, Qumsyieh M, Ward DC.

Lab Invest. 2001 Apr;81(4):475-81.

PMID:
11304566
20.

Characterization of Japanese flounder karyotype by chromosome bandings and fluorescence in situ hybridization with DNA markers.

Fujiwara A, Fujiwara M, Nishida-Umehara C, Abe S, Masaoka T.

Genetica. 2007 Nov;131(3):267-74. Epub 2007 Feb 2.

PMID:
17273899

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