Midro AT - Search Results

1

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: midro at. Genet Couns. 2006;17(2):211-8. Genet Couns. 2006. PMID: 16970040

2

TAR syndrome with orofacial clefting.

Midro A, Hubert E, Preferansow J, Iwaszkiewicz-Pawłowska A. Midro A, et al. Genet Couns. 1993;4(3):187-92. Genet Couns. 1993. PMID: 8267925

3

Floating Harbor syndrome. Case report and further syndrome delineation.

Midro AT, Olchowik B, Rogowska M, Hubert E, Hassman-Poznańska E, Papasz A, Szulc S, Wiśniewski A. Midro AT, et al. Ann Genet. 1997;40(3):133-8. Ann Genet. 1997. PMID: 9401100

4

Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2.

Panasiuk B, Danik J, Lurie IW, Stasiewicz-Jarocka B, Leśniewicz R, Sawicka A, Kałuzewski B, Midro AT. Panasiuk B, et al. Among authors: midro at. Adv Med Sci. 2009;54(2):203-10. doi: 10.2478/v10039-009-0024-5. Adv Med Sci. 2009. PMID: 19758973

5

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: midro at. 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

6

Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome.

Midro AT, Panasiuk B, Tümer Z, Stankiewicz P, Silahtaroglu A, Lupski JR, Zemanova Z, Stasiewicz-Jarocka B, Hubert E, Tarasów E, Famulski W, Zadrozna-Tołwińska B, Wasilewska E, Kirchhoff M, Kalscheuer V, Michalova K, Tommerup N. Midro AT, et al. Am J Med Genet A. 2004 Jan 15;124A(2):179-91. doi: 10.1002/ajmg.a.20367. Am J Med Genet A. 2004. PMID: 14699618 Review.

7

Familial occurrence of isodicentric X chromosomes with different breakpoints.

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

8

Midro AT, Stasiewicz-Jarocka B, Borys J, Hubert E, Skotnicka B, Hassmann-Poznańska E, Sierpińska T, Panasiuk B, Schanze D, Zenker M. Midro AT, et al. Am J Med Genet A. 2020 Apr;182(4):773-779. doi: 10.1002/ajmg.a.61495. Epub 2020 Jan 30. Am J Med Genet A. 2020. PMID: 31999076

9

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: midro at. Adv Med Sci. 2007;52 Suppl 1:166-70. Adv Med Sci. 2007. PMID: 18229657

10

[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. Pol Tyg Lek. 1987 Mar 2;42(9):260-3. Pol Tyg Lek. 1987. PMID: 3601789 Polish. No abstract available.

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