Latos-Bieleńska A - Search Results

1

Mutation screening of Charcot-Marie-Tooth patients in Poland.

Kochański A, Timmerman V, Jedrzejowska H, Ryniewicz B, Löfgren A, De Vriendt E, Van Broeckhoven C, Latos-Bieleńska A, Hausmanowa-Petrusewicz I. Kochański A, et al. Ann N Y Acad Sci. 1999 Sep 14;883:493-6. Ann N Y Acad Sci. 1999. PMID: 10586282 No abstract available.

2

A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease.

Kochanski A, Lofgren A, Jedrzejowska H, Ryniewicz B, Czarny-Ratajczak M, Barciszewska A, Samocko J, Hausmanowa-Petrusewicz I, De Jonghe P, Timmerman V, Latos-Bielenska A. Kochanski A, et al. Hum Mutat. 2001 Feb;17(2):157. doi: 10.1002/1098-1004(200102)17:2<157::AID-HUMU22>3.0.CO;2-E. Hum Mutat. 2001. PMID: 11180613 No abstract available.

3

Mutation Screening of Charcot-Marie-Tooth Patients in Poland.

Kochański A, Timmerman V, Jedrzejowska H, Ryniewicz B, Löfgren A, De Vriendt E, VAN Broeckhoven C, Latos-Bieleńska A, Hausmanowa-Petrusewicz I. Kochański A, et al. Ann N Y Acad Sci. 1999 Oct;883(1):493-496. doi: 10.1111/j.1749-6632.1999.tb08619.x. Ann N Y Acad Sci. 1999. PMID: 29086975 No abstract available.

4

DNA damage induced by lithotripter generated shock waves: short report.

Kochański AM, Mejnartowicz JP, Latos-Bieleńska A, Etienne J, Filipczyńiski L. Kochański AM, et al. Int Urol Nephrol. 2001;32(3):419-22. doi: 10.1023/a:1017527611798. Int Urol Nephrol. 2001. PMID: 11583365

5

Refinement of localization of the human genes for myeloperoxidase (MPO), protein kinase C, alpha polypeptide, PRKCA, and the DNA fragment D17S21 on chromosome 17q.

Latos-Bielenska A, Klett C, Just W, Hameister H. Latos-Bielenska A, et al. Hereditas. 1991;115(1):69-72. doi: 10.1111/j.1601-5223.1991.tb00348.x. Hereditas. 1991. PMID: 1663499 Free article.

6

Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.

Wozniak A, Wolnik-Brzozowska D, Wisniewska M, Glazar R, Materna-Kiryluk A, Moszura T, Badura-Stronka M, Skolozdrzy J, Krawczynski MR, Zeyland J, Bobkowski W, Slomski R, Latos-Bielenska A, Siwinska A. Wozniak A, et al. BMC Pediatr. 2010 Dec 6;10:88. doi: 10.1186/1471-2431-10-88. BMC Pediatr. 2010. PMID: 21134246 Free PMC article.

7

Idiopathic infertility in married couples in the light of cytogenetic analysis and sperm penetration assay.

Wiland E, Wojda A, Kamieniczna M, Latos-Bieleńska A, Jedrzejczak P, Kurpisz M. Wiland E, et al. Folia Histochem Cytobiol. 2001;39(1):35-41. Folia Histochem Cytobiol. 2001. PMID: 11261547

8

Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndrome.

Budny B, Badura-Stronka M, Materna-Kiryluk A, Tzschach A, Raynaud M, Latos-Bielenska A, Ropers HH. Budny B, et al. Clin Genet. 2010 Jun;77(6):541-51. doi: 10.1111/j.1399-0004.2010.01429.x. Epub 2010 Apr 19. Clin Genet. 2010. PMID: 20412111

9

Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses.

Jamsheer A, Socha M, Sowińska-Seidler A, Telega K, Trzeciak T, Latos-Bieleńska A. Jamsheer A, et al. J Appl Genet. 2014 May;55(2):183-8. doi: 10.1007/s13353-014-0195-z. Epub 2014 Feb 15. J Appl Genet. 2014. PMID: 24532482 Free PMC article.

10

Subtle familial translocation t(11;22)(q24.2;q13.33) resulting in Jacobsen syndrome and distal trisomy 22q13.3: further details of genotype-phenotype maps.

Jamsheer A, Smyk M, Wierzba J, Kołowska J, Woźniak A, Skołozdrzy J, Fischer M, Latos-Bieleńska A. Jamsheer A, et al. J Appl Genet. 2008;49(4):397-405. doi: 10.1007/BF03195639. J Appl Genet. 2008. PMID: 19029687

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

164 results

Search Page

Filters