Sawicka A - Search Results

1

Second observation of Silver-Russel syndrome in a carrier of a reciprocal translocation with one breakpoint at site 17q25.

Midro AT, Debek K, Sawicka A, Marcinkiewicz D, Rogowska M. Midro AT, et al. Among authors: sawicka a. Clin Genet. 1993 Jul;44(1):53-5. doi: 10.1111/j.1399-0004.1993.tb03845.x. Clin Genet. 1993. PMID: 8403458 No abstract available.

2

Familial occurrence of isodicentric X chromosomes with different breakpoints.

Midro AT, Kulikowski M, Sawicka A, Panasiuk B, Korsak E. Midro AT, et al. Among authors: sawicka a. Clin Genet. 1988 Sep;34(3):153-60. doi: 10.1111/j.1399-0004.1988.tb02855.x. Clin Genet. 1988. PMID: 3180502

3

[A case of a girl with a ring chromosome 18 in the karyotype].

Midro AT, Czerwińska-Ciechan K, Wiśniewski L, Sawicka A, Marcinkiewicz D. Midro AT, et al. Among authors: sawicka a. Pol Tyg Lek. 1987 Mar 2;42(9):260-3. Pol Tyg Lek. 1987. PMID: 3601789 Polish. No abstract available.

4

[Familial translocation t (9;16) in a patient with irregular menstrual cycles].

Sledziewski A, Midro AT, Sawicka A. Sledziewski A, et al. Among authors: sawicka a. Ginekol Pol. 1996 Jun;67(6):313-6. Ginekol Pol. 1996. PMID: 9138988 Polish.

5

[Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH].

Sawicka A, Leśniewicz R, Zawada M, Stasiewicz-Jarocka B, Midro AT. Sawicka A, et al. Ginekol Pol. 1998 Apr;69(4):200-6. Ginekol Pol. 1998. PMID: 9640866 Polish.

6

[Pedigree analysis of childless families of reciprocal chromosome translocation carriers].

Stasiewicz-Jarocka B, Panasiuk B, Sawicka A, Leśniewicz R, Midro AT. Stasiewicz-Jarocka B, et al. Among authors: sawicka a. Ginekol Pol. 1998 Dec;69(12):1183-90. Ginekol Pol. 1998. PMID: 10224801 Polish.

7

XYY syndrome and acute myeloblastic leukemia.

Midro AT, Wojtukiewicz M, Bielawiec M, Sawicka A. Midro AT, et al. Among authors: sawicka a. Cancer Genet Cytogenet. 1987 Feb;24(2):363-5. doi: 10.1016/0165-4608(87)90120-8. Cancer Genet Cytogenet. 1987. PMID: 3466685

8

Translocation form of Wolf-Hirschhorn syndrome --assessment of recurrence rate probability.

Panasiuk B, Leśniewicz R, Spółczyńska A, Myśliwiec M, de Die Smulders Ch, Sawicka A, Midro AT. Panasiuk B, et al. Among authors: sawicka a. Adv Med Sci. 2007;52 Suppl 1:166-70. Adv Med Sci. 2007. PMID: 18229657

9

Partial trisomy of long arm of chromosome 4 as a result of dir dup (4)(q27q31.3) de novo.

Hubert E, Sawicka A, Wasilewska E, Midro AT. Hubert E, et al. Among authors: sawicka a. Genet Couns. 2006;17(2):211-8. Genet Couns. 2006. PMID: 16970040

10

Clonal chromosomal aberrations in Philadelphia negative cells such as monosomy 7 and trisomy 8 may persist for years with no impact on the long term outcome in patients with chronic myeloid leukemia.

Wasilewska EM, Panasiuk B, Gniot M, Sawicka A, Kozłowska K, Lewandowski K, Kłoczko J, Midro AT. Wasilewska EM, et al. Among authors: sawicka a. Cancer Genet. 2017 Oct;216-217:1-9. doi: 10.1016/j.cancergen.2017.04.066. Epub 2017 Apr 28. Cancer Genet. 2017. PMID: 29025581

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