Kardas I - Search Results

1

Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.

Panagopoulos I, Mertens F, Dêbiec-Rychter M, Isaksson M, Limon J, Kardas I, Domanski HA, Sciot R, Perek D, Crnalic S, Larsson O, Mandahl N. Panagopoulos I, et al. Among authors: kardas i. Int J Cancer. 2002 Jun 1;99(4):560-7. doi: 10.1002/ijc.10404. Int J Cancer. 2002. PMID: 11992546 Free article.

2

Cytogenetic and molecular findings in 75 clear cell renal cell carcinomas.

Kardas I, Mrózek K, Babinska M, Krajka K, Hadaczek P, Lubinski J, Roszkiewicz A, Kuziemska E, Limon J. Kardas I, et al. Oncol Rep. 2005 May;13(5):949-56. Oncol Rep. 2005. PMID: 15809763

3

Translocation (X;1)(p11.2;q21) in a papillary renal cell carcinoma in a 14-year-old girl.

Kardaś I, Denis A, Babińska M, Gronwald J, Podolski J, Zajaczek S, Kram A, Lubiński J, Limon J. Kardaś I, et al. Cancer Genet Cytogenet. 1998 Mar;101(2):159-61. doi: 10.1016/s0165-4608(97)00266-5. Cancer Genet Cytogenet. 1998. PMID: 9494621

4

A girl with duplication 9q34 syndrome.

Gawlik-Kuklinska K, Iliszko M, Wozniak A, Debiec-Rychter M, Kardas I, Wierzba J, Limon J. Gawlik-Kuklinska K, et al. Among authors: kardas i. Am J Med Genet A. 2007 Sep 1;143A(17):2019-23. doi: 10.1002/ajmg.a.31847. Am J Med Genet A. 2007. PMID: 17663474

5

Retrospective analysis of prognostic significance of the estrogen-inducible pS2 gene in male breast carcinoma.

Kardaś I, Seitz G, Limon J, Niezabitowski A, Ryś J, Theisinger B, Welter C, Blin N. Kardaś I, et al. Cancer. 1993 Sep 1;72(5):1652-6. doi: 10.1002/1097-0142(19930901)72:5<1652::aid-cncr2820720526>3.0.co;2-4. Cancer. 1993. PMID: 8394203

6

Partial trisomy of distal 5q and partial monosomy of Xp as a result of mating between two translocation carriers: a female with a balanced translocation t(X;5)(p11;q31) and a male with a der(13;14)(q10;q10)--a case report and a family study.

Wysocka B, Brozek I, Wierzba J, Kardaś I, Woźniak A, Kowalczyk J, Balcerska A, Limon J. Wysocka B, et al. Among authors: kardas i. Ann Genet. 2002 Jul-Sep;45(3):143-6. doi: 10.1016/s0003-3995(02)01124-3. Ann Genet. 2002. PMID: 12381446

7

Cornelia de Lange syndrome associated with a de-novo novel NIPBL splice-site mutation and a coincidental inherited translocation t(3;5)(p13;q11).

Wierzba J, Kuzniacka A, Ratajska M, Lipska BS, Kardas I, Iliszko M, Limon J. Wierzba J, et al. Among authors: kardas i. Clin Dysmorphol. 2011 Oct;20(4):222-224. doi: 10.1097/MCD.0b013e3283455175. Clin Dysmorphol. 2011. PMID: 21666440 No abstract available.

8

Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia.

Brozek I, Babińska M, Kardaś I, Woźniak A, Balcerska A, Hellmann A, Limon J. Brozek I, et al. Among authors: kardas i. J Appl Genet. 2003;44(3):401-12. J Appl Genet. 2003. PMID: 12923315

9

HER2 Amplification Has no Prognostic Value in Sporadic and Hereditary Ovarian Tumours.

Brozek I, Kardaś I, Ochman K, Debniak J, Stukan M, Ratajska M, Morzuch L, Emerich J, Limon J. Brozek I, et al. Among authors: kardas i. Hered Cancer Clin Pract. 2006 Nov 15;4(1):39-42. doi: 10.1186/1897-4287-4-1-39. Hered Cancer Clin Pract. 2006. PMID: 20223002 Free PMC article.

10

Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.

Stankiewicz P, Brozek I, Hélias-Rodzewicz Z, Wierzba J, Pilch J, Bocian E, Balcerska A, Wozniak A, Kardaś I, Wirth J, Mazurczak T, Limon J. Stankiewicz P, et al. Among authors: kardas i. Am J Med Genet. 2001 Jul 1;101(3):226-39. doi: 10.1002/1096-8628(20010701)101:3<226::aid-ajmg1349>3.0.co;2-#. Am J Med Genet. 2001. PMID: 11424138

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