Nowakowska BA - Search Results

1

Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss.

Kowalczyk K, Smyk M, Bartnik-Głaska M, Plaskota I, Wiśniowiecka-Kowalnik B, Bernaciak J, Chojnacka M, Paczkowska M, Niemiec M, Dutkiewicz D, Kozar A, Magdziak R, Krawczyk W, Pietras G, Michalak E, Klepacka T, Obersztyn E, Bal J, Nowakowska BA. Kowalczyk K, et al. Among authors: nowakowska ba. J Assist Reprod Genet. 2022 Feb;39(2):357-367. doi: 10.1007/s10815-022-02400-8. Epub 2022 Jan 26. J Assist Reprod Genet. 2022. PMID: 35079943 Free PMC article.

2

[[Chimerism and tolerance].

Nowakowska B. Nowakowska B. Postepy Hig Med Dosw. 1999;53(6):771-83. Postepy Hig Med Dosw. 1999. PMID: 10737038 Review. Polish.

3

[Problems with donor-recipient matching in kidney and bone marrow transplantation].

Nowakowska B. Nowakowska B. Postepy Hig Med Dosw. 1995;49(1):107-15. Postepy Hig Med Dosw. 1995. PMID: 8657608 Review. Polish.

4

[Pregnancy, micro-chimerism and autoimmune diseases].

Nowakowska B. Nowakowska B. Postepy Hig Med Dosw. 2002;56(2):127-37. Postepy Hig Med Dosw. 2002. PMID: 12107958 Review. Polish.

5

[Rejection of allogeneic bone marrow transplant. Case report].

Szczylik C, Ratajczak M, Dumański Z, Myc A, Siekierzyński M, Rybicki Z, Kłos M, Zaboklicki S, Zaborowski P, Nowakowska B, et al. Szczylik C, et al. Pol Arch Med Wewn. 1988 Jan;79(1):30-7. Pol Arch Med Wewn. 1988. PMID: 3275168 Polish.

6

Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3).

Bocian E, Suchenek K, Obersztyn E, Nowakowska B, Mazurczak T. Bocian E, et al. J Appl Genet. 2005;46(1):109-14. J Appl Genet. 2005. PMID: 15741672

7

[Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].

Bocian E, Nowakowska B, Obersztyn E, Borg K, Chudoba I, Kostyk E, Kruczek A, Pietrzyk J, Mazurczak T. Bocian E, et al. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):211-25. Med Wieku Rozwoj. 2006. PMID: 17028390 Polish.

8

[Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities].

Borg K, Bocian E, Stankiewicz P, Obersztyn E, Kruczek A, Nowakowska B, Ilnicka A, Mazurczak T. Borg K, et al. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):227-46. Med Wieku Rozwoj. 2006. PMID: 17028391 Polish.

9

Recurrent SOX9 deletion campomelic dysplasia due to somatic mosaicism in the father.

Smyk M, Obersztyn E, Nowakowska B, Bocian E, Cheung SW, Mazurczak T, Stankiewicz P. Smyk M, et al. Am J Med Genet A. 2007 Apr 15;143A(8):866-70. doi: 10.1002/ajmg.a.31631. Am J Med Genet A. 2007. PMID: 17352389

10

A girl with deletion 9q22.1-q22.32 including the PTCH and ROR2 genes identified by genome-wide array-CGH.

Nowakowska B, Kutkowska-Kaźmierczak A, Stankiewicz P, Bocian E, Obersztyn E, Ou Z, Cheung SW, Cai WW. Nowakowska B, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1885-9. doi: 10.1002/ajmg.a.31845. Am J Med Genet A. 2007. PMID: 17632781

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