Nowakowska B - Search Results

1

Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3.

Kutkowska-Kaźmierczak A, Boczar M, Kalka E, Castañeda J, Klapecki J, Pietrzyk A, Barczyk A, Malinowska O, Landowska A, Gambin T, Kowalczyk K, Wiśniowiecka-Kowalnik B, Smyk M, Dawidziuk M, Niepokój K, Paczkowska M, Szyld P, Lipska-Ziętkiewicz B, Szczałuba K, Kostyk E, Runge A, Rutkowska K, Płoski R, Nowakowska B, Bal J, Obersztyn E, Gos M. Kutkowska-Kaźmierczak A, et al. Among authors: nowakowska b. Genes (Basel). 2021 Aug 17;12(8):1257. doi: 10.3390/genes12081257. Genes (Basel). 2021. PMID: 34440431 Free PMC article.

2

[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.

3

[[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.

4

[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.

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. Among authors: nowakowska b. 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. Among authors: nowakowska b. 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. Among authors: nowakowska b. 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. Among authors: nowakowska b. 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. Among authors: nowakowska b. 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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