Nowakowska B - Search Results

1

Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations.

Ou Z, Jarmuz M, Sparagana SP, Michaud J, Décarie JC, Yatsenko SA, Nowakowska B, Furman P, Shaw CA, Shaffer LG, Lupski JR, Chinault AC, Cheung SW, Stankiewicz P. Ou Z, et al. Among authors: nowakowska b. Hum Genet. 2006 Sep;120(2):227-37. doi: 10.1007/s00439-006-0200-7. Epub 2006 Jun 22. Hum Genet. 2006. PMID: 16791615

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

[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.

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

[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.

6

[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.

7

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

8

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

9

Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation.

Borg K, Nowakowska B, Obersztyn E, Cheung SW, Brycz-Witkowska J, Korniszewski L, Mazurczak T, Stankiewicz P, Bocian E. Borg K, et al. Among authors: nowakowska b. Am J Med Genet A. 2007 Nov 15;143A(22):2738-43. doi: 10.1002/ajmg.a.32017. Am J Med Genet A. 2007. PMID: 17937435

10

Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections.

Smyk M, Obersztyn E, Nowakowska B, Nawara M, Cheung SW, Mazurczak T, Stankiewicz P, Bocian E. Smyk M, et al. Among authors: nowakowska b. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):799-806. doi: 10.1002/ajmg.b.30683. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18165974

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