Silahtaroglu A - Search Results

1

Breakpoints around the HOXD cluster result in various limb malformations.

Dlugaszewska B, Silahtaroglu A, Menzel C, Kübart S, Cohen M, Mundlos S, Tümer Z, Kjaer K, Friedrich U, Ropers HH, Tommerup N, Neitzel H, Kalscheuer VM. Dlugaszewska B, et al. Among authors: silahtaroglu a. J Med Genet. 2006 Feb;43(2):111-8. doi: 10.1136/jmg.2005.033555. Epub 2005 Jun 24. J Med Genet. 2006. PMID: 15980115 Free PMC article.

2

A small supernumerary marker chromosome X identified by in situ hybridization.

Silahtaroglu AN, Hacihanefioglu S, Yilmaz S, Tarkan Y, Cenani A, Tümer Z. Silahtaroglu AN, et al. Clin Genet. 1995 May;47(5):270-3. doi: 10.1111/j.1399-0004.1995.tb04310.x. Clin Genet. 1995. PMID: 7554355

3

Assignment of the human gene for pregnancy-associated plasma protein A (PAPPA) to 9q33.1 by fluorescence in situ hybridization to mitotic and meiotic chromosomes.

Silahtaroglu AN, Tümer Z, Kristensen T, Sottrup-Jensen L, Tommerup N. Silahtaroglu AN, et al. Cytogenet Cell Genet. 1993;62(4):214-6. doi: 10.1159/000133479. Cytogenet Cell Genet. 1993. PMID: 7679961

4

Characterization of a supernumerary small marker X chromosome in two females with similar phenotypes.

Tümer Z, Wolff D, Silahtaroglu AN, Orum A, Brøndum-Nielsen K. Tümer Z, et al. Among authors: silahtaroglu an. Am J Med Genet. 1998 Feb 26;76(1):45-50. Am J Med Genet. 1998. PMID: 9508064

5

Not para-, not peri-, but centric inversion of chromosome 12.

Silahtaroglu AN, Hacihanefioglu S, Güven GS, Cenani A, Wirth J, Tommerup N, Tümer Z. Silahtaroglu AN, et al. J Med Genet. 1998 Aug;35(8):682-4. doi: 10.1136/jmg.35.8.682. J Med Genet. 1998. PMID: 9719380 Free PMC article.

6

Isolation of the human beaded-filament structural protein 1 gene (BFSP1) and assignment to chromosome 20p11.23-p12.1.

Rendtorff ND, Hansen C, Silahtaroglu A, Henriksen KF, Tommerup N. Rendtorff ND, et al. Among authors: silahtaroglu a. Genomics. 1998 Oct 1;53(1):114-6. doi: 10.1006/geno.1998.5478. Genomics. 1998. PMID: 9787085 No abstract available.

7

Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome.

Silahtaroglu A, Hol FA, Jensen PK, Erdel M, Duba HC, Geurds MP, Knoers NV, Mariman EC, Tümer Z, Utermann G, Wirth J, Bugge M, Tommerup N. Silahtaroglu A, et al. Eur J Hum Genet. 1999 Jan;7(1):68-76. doi: 10.1038/sj.ejhg.5200260. Eur J Hum Genet. 1999. PMID: 10094193

8

Assignment of the NR2E3 gene to mouse chromosome 9 and to human chromosome 15q22.33-->q23.

Rendtorff ND, Vissing H, Tümer Z, Silahtaroglu A, Tommerup N. Rendtorff ND, et al. Among authors: silahtaroglu a. Cytogenet Cell Genet. 2000;89(3-4):279-80. doi: 10.1159/000015635. Cytogenet Cell Genet. 2000. PMID: 10965145 No abstract available.

9

MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern.

Nielsen JB, Henriksen KF, Hansen C, Silahtaroglu A, Schwartz M, Tommerup N. Nielsen JB, et al. Among authors: silahtaroglu a. Eur J Hum Genet. 2001 Mar;9(3):178-84. doi: 10.1038/sj.ejhg.5200600. Eur J Hum Genet. 2001. PMID: 11313756

10

Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes.

Poulsen TS, Silahtaroglu AN, Gisselø CG, Gaarsdal E, Rasmussen T, Tommerup N, Johnsen HE. Poulsen TS, et al. Among authors: silahtaroglu an. Genes Chromosomes Cancer. 2001 Nov;32(3):265-74. doi: 10.1002/gcc.1193. Genes Chromosomes Cancer. 2001. PMID: 11579466

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