Stembalska A - Search Results

1

[Familial chromosome X structural aberrations - case report].

Stembalska A, Barg E, Jakiel A, Sasiadek MM. Stembalska A, et al. Pediatr Endocrinol Diabetes Metab. 2010;16(4):310-4. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 21447275 Polish.

2

[Rapid-FISH--fast and reliable method of detecting common numerical chromosomal aberrations in prenatal diagnosis].

Laczmańska I, Stembalska A, Slezak R, Kozłowska J, Makowska I, Czemarmazowicz H, Pesz KA, Smigiel R, Jakiel A, Sasiadek MM. Laczmańska I, et al. Among authors: stembalska a. Ginekol Pol. 2007 Dec;78(12):952-5. Ginekol Pol. 2007. PMID: 18411918 Polish.

3

[Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology].

Laczmańska I, Jakubiak A, Slęzak R, Pesz K, Stembalska A, Laczmański L, Sąsiadek MM, Smigiel R. Laczmańska I, et al. Among authors: stembalska a. Med Wieku Rozwoj. 2011 Apr-Jun;15(2):132-9. Med Wieku Rozwoj. 2011. PMID: 22002044 Polish.

4

Clinical Observation of a Child with Prenatally Diagnosed De Novo Partial Trisomy of Chromosome 20.

Stembalska A, Gil J, Laczmanska I, Sasiadek M. Stembalska A, et al. Fetal Pediatr Pathol. 2019 Jun;38(3):245-256. doi: 10.1080/15513815.2019.1576818. Epub 2019 Mar 20. Fetal Pediatr Pathol. 2019. PMID: 30893560

5

Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.

Laczmanska I, Stembalska A, Gil J, Czemarmazowicz H, Sasiadek M. Laczmanska I, et al. Among authors: stembalska a. Eur J Med Genet. 2006 Jan-Feb;49(1):87-92. doi: 10.1016/j.ejmg.2005.04.023. Epub 2005 Jul 6. Eur J Med Genet. 2006. PMID: 16473315

6

8q22-->qter duplication in a child with multiple congenital malformations: case report.

Sasiadek M, Stembalska A, Schlade K, Zych M. Sasiadek M, et al. Among authors: stembalska a. Med Sci Monit. 2000 Jan-Feb;6(1):141-4. Med Sci Monit. 2000. PMID: 11208302 Free article.

7

Three distinct regions of deletion on 13q in squamous cell carcinoma of the larynx.

Stembalska A, Blin N, Ramsey D, Sasiadek MM. Stembalska A, et al. Oncol Rep. 2006 Aug;16(2):417-21. Oncol Rep. 2006. PMID: 16820925

8

Recombinant chromosome 4 resulting from a maternal pericentric inversion in two sisters presenting consistent dysmorphic features.

Stembalska A, Laczmanska I, Schlade-Bartusiak K, Czemarmazowicz H, Murawski M, Sasiadek M. Stembalska A, et al. Eur J Pediatr. 2007 Jan;166(1):67-71. doi: 10.1007/s00431-006-0214-0. Epub 2006 Sep 30. Eur J Pediatr. 2007. PMID: 17013597

9

Cyclin D1 and MLH1 levels in laryngeal cancer are linked to chromosomal imbalance.

Sasiadek MM, Smigiel R, Stembalska A, Ramsey D, Blin N. Sasiadek MM, et al. Among authors: stembalska a. Anticancer Res. 2006 Nov-Dec;26(6B):4597-601. Anticancer Res. 2006. PMID: 17201183 Free article.

10

Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations.

Laczmanska I, Gil J, Karpinski P, Stembalska A, Trusewicz A, Pesz K, Ramsey D, Schlade-Bartusiak K, Blin N, Sasiadek MM. Laczmanska I, et al. Among authors: stembalska a. Environ Mol Mutagen. 2007 Oct;48(8):666-71. doi: 10.1002/em.20333. Environ Mol Mutagen. 2007. PMID: 17685459

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