Stembalska A - Search Results

1

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

2

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

3

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

4

Prenatal diagnosis--principles of diagnostic procedures and genetic counseling.

Stembalska A, Slezak R, Pesz K, Gil J, Sasiadek M. Stembalska A, et al. Folia Histochem Cytobiol. 2007;45 Suppl 1:S11-6. Folia Histochem Cytobiol. 2007. PMID: 18292841 Review.

5

[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.

6

Cancer stem cells: the theory and perspectives in cancer therapy.

Gil J, Stembalska A, Pesz KA, Sasiadek MM. Gil J, et al. Among authors: stembalska a. J Appl Genet. 2008;49(2):193-9. doi: 10.1007/BF03195612. J Appl Genet. 2008. PMID: 18436993 Review.

7

Irrelevance of CHEK2 variants to diagnosis of breast/ovarian cancer predisposition in Polish cohort.

Myszka A, Karpinski P, Slezak R, Czemarmazowicz H, Stembalska A, Gil J, Laczmanska I, Bednarczyk D, Szmida E, Sasiadek MM. Myszka A, et al. Among authors: stembalska a. J Appl Genet. 2011 May;52(2):185-91. doi: 10.1007/s13353-010-0013-1. Epub 2010 Dec 1. J Appl Genet. 2011. PMID: 21120647

8

[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.

9

[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.

10

[Rett syndrome. Classical form and preserved speech variant as a different phenotype effect of deletion with the same starting point in MeCP2 gene - report of 2 cases].

Stembalska A, Gil J, Pesz KA. Stembalska A, et al. Med Wieku Rozwoj. 2011 Oct-Dec;15(4):445-50. Med Wieku Rozwoj. 2011. PMID: 22516699 Polish.

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