Collin A - Search Results

1

Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.

Davidsson J, Collin A, Björkhem G, Soller M. Davidsson J, et al. Among authors: collin a. BMC Med Genet. 2008 Jan 14;9:2. doi: 10.1186/1471-2350-9-2. BMC Med Genet. 2008. PMID: 18194513 Free PMC article.

2

Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12.

Davidsson J, Collin A, Oreberg M, Gisselsson D. Davidsson J, et al. Among authors: collin a. Clin Genet. 2008 Jan;73(1):44-9. doi: 10.1111/j.1399-0004.2007.00917.x. Epub 2007 Nov 13. Clin Genet. 2008. PMID: 18005181

3

Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: an array-based genotype-phenotype correlation and a comprehensive review of previously published cases.

Davidsson J, Collin A, Olsson ME, Lundgren J, Soller M. Davidsson J, et al. Among authors: collin a. Epilepsy Res. 2008 Sep;81(1):69-79. doi: 10.1016/j.eplepsyres.2008.04.018. Epub 2008 Jun 9. Epilepsy Res. 2008. PMID: 18539002

4

dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome.

Davidsson J, Jahnke K, Forsgren M, Collin A, Soller M. Davidsson J, et al. Among authors: collin a. Obesity (Silver Spring). 2010 Mar;18(3):580-7. doi: 10.1038/oby.2009.298. Epub 2009 Sep 17. Obesity (Silver Spring). 2010. PMID: 19763090 Free article.

5

False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.

Collin A, Sladkevicius P, Soller M. Collin A, et al. Prenat Diagn. 2009 Dec;29(13):1279-81. doi: 10.1002/pd.2401. Prenat Diagn. 2009. PMID: 19911414 No abstract available.

6

Unstable translocation (8;22) in a case of giant cell reparative granuloma.

Johnsson A, Collin A, Rydholm A, Domanski HA, Mertens F, Mandahl N. Johnsson A, et al. Among authors: collin a. Cancer Genet Cytogenet. 2007 Aug;177(1):59-63. doi: 10.1016/j.cancergencyto.2007.04.017. Cancer Genet Cytogenet. 2007. PMID: 17693193

7

Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.

Bartuma H, Möller E, Collin A, Domanski HA, Von Steyern FV, Mandahl N, Mertens F. Bartuma H, et al. Among authors: collin a. Cancer Genet Cytogenet. 2010 Jun;199(2):143-6. doi: 10.1016/j.cancergencyto.2010.02.011. Cancer Genet Cytogenet. 2010. PMID: 20471519 Free article.

8

Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype.

Bartuma H, Hallor KH, Panagopoulos I, Collin A, Rydholm A, Gustafson P, Bauer HC, Brosjö O, Domanski HA, Mandahl N, Mertens F. Bartuma H, et al. Among authors: collin a. Genes Chromosomes Cancer. 2007 Jun;46(6):594-606. doi: 10.1002/gcc.20445. Genes Chromosomes Cancer. 2007. PMID: 17370328

9

Clinical variability of Waardenburg-Shah syndrome in patients with proximal 13q deletion syndrome including the endothelin-B receptor locus.

Tüysüz B, Collin A, Arapoğlu M, Suyugül N. Tüysüz B, et al. Among authors: collin a. Am J Med Genet A. 2009 Oct;149A(10):2290-5. doi: 10.1002/ajmg.a.33031. Am J Med Genet A. 2009. PMID: 19764031

10

Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.

Bartuma H, Panagopoulos I, Collin A, Trombetta D, Domanski HA, Mandahl N, Mertens F. Bartuma H, et al. Among authors: collin a. Mol Cancer. 2009 Jun 9;8:36. doi: 10.1186/1476-4598-8-36. Mol Cancer. 2009. PMID: 19508721 Free PMC article.

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