Schlade-Bartusiak K - Search Results

1

Bleomycin-induced chromosome aberrations in head and neck cancer patients analyzed by classical cytogenetics and FISH.

Zych M, Schlade-Bartusiak K, Chorostkowska A, Stembalska A, Krêcicki T, Sasiadek M. Zych M, et al. Cancer Lett. 2000 May 1;152(2):123-7. doi: 10.1016/s0304-3835(99)00411-5. Cancer Lett. 2000. PMID: 10773402

2

Significant involvement of chromosome 13q deletions in progression of larynx cancer, detected by comparative genomic hybridization.

Schlade-Bartusiak K, Stembalska A, Ramsey D. Schlade-Bartusiak K, et al. J Appl Genet. 2005;46(4):407-13. J Appl Genet. 2005. PMID: 16278516

3

Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations.

Laczmanska I, Gil J, Karpinski P, Stembalska A, Trusewicz A, Pesz K, Ramsey D, Schlade-Bartusiak K, Blin N, Sasiadek MM. Laczmanska I, et al. Environ Mol Mutagen. 2007 Oct;48(8):666-71. doi: 10.1002/em.20333. Environ Mol Mutagen. 2007. PMID: 17685459

4

The influence of GSTM1 and GSTT1 genotypes on the induction of sister chromatid exchanges and chromosome aberrations by 1,2:3,4-diepoxybutane.

Schlade-Bartusiak K, Sasiadek M, Kozlowska J. Schlade-Bartusiak K, et al. Mutat Res. 2000 Feb 16;465(1-2):69-75. doi: 10.1016/s1383-5718(99)00213-2. Mutat Res. 2000. PMID: 10708971

5

FISH-mapping of telomeric 14q32 deletions: search for the cause of seizures.

Schlade-Bartusiak K, Costa T, Summers AM, Nowaczyk MJ, Cox DW. Schlade-Bartusiak K, et al. Am J Med Genet A. 2005 Oct 15;138A(3):218-24. doi: 10.1002/ajmg.a.30942. Am J Med Genet A. 2005. PMID: 16152642

6

A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlations.

Schlade-Bartusiak K, Ardinger H, Cox DW. Schlade-Bartusiak K, et al. Am J Med Genet A. 2009 May;149A(5):1012-8. doi: 10.1002/ajmg.a.32752. Am J Med Genet A. 2009. PMID: 19365838

7

A child with deletion (14)(q24.3q32.13) and auditory neuropathy.

Schlade-Bartusiak K, Macintyre G, Zunich J, Cox DW. Schlade-Bartusiak K, et al. Am J Med Genet A. 2008 Jan 1;146A(1):117-23. doi: 10.1002/ajmg.a.32064. Am J Med Genet A. 2008. PMID: 18074379

8

A minigene approach for analysis of ATP7B splice variants in patients with Wilson disease.

Wilson AM, Schlade-Bartusiak K, Tison JL, Macintyre G, Cox DW. Wilson AM, et al. Biochimie. 2009 Oct;91(10):1342-5. doi: 10.1016/j.biochi.2009.06.008. Epub 2009 Jun 21. Biochimie. 2009. PMID: 19540904

9

Brain MRI abnormalities and spectrum of neurological and clinical findings in three patients with proximal 16p11.2 microduplication.

Filges I, Sparagana S, Sargent M, Selby K, Schlade-Bartusiak K, Lueder GT, Robichaux-Viehoever A, Schlaggar BL, Shimony JS, Shinawi M. Filges I, et al. Among authors: schlade bartusiak k. Am J Med Genet A. 2014 Aug;164A(8):2003-12. doi: 10.1002/ajmg.a.36605. Epub 2014 May 28. Am J Med Genet A. 2014. PMID: 24891046

10

Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p.

Schlade-Bartusiak K, Tucker T, Safavi H, Livingston J, van Allen MI, Eydoux P, Armstrong L. Schlade-Bartusiak K, et al. Eur J Med Genet. 2013 May;56(5):229-35. doi: 10.1016/j.ejmg.2013.01.013. Epub 2013 Feb 14. Eur J Med Genet. 2013. PMID: 23416622

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