Tastemir D - Search Results

1

A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies.

Demirhan O, Türkmen S, Schwabe GC, Soyupak S, Akgül E, Tastemir D, Karahan D, Mundlos S, Lehmann K. Demirhan O, et al. Among authors: tastemir d. J Med Genet. 2005 Apr;42(4):314-7. doi: 10.1136/jmg.2004.023564. J Med Genet. 2005. PMID: 15805157 Free PMC article.

2

Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.

Demirhan O, Tastemir D. Demirhan O, et al. Among authors: tastemir d. Fertil Steril. 2006 Jul;86(1):219.e15-9. doi: 10.1016/j.fertnstert.2005.11.077. Fertil Steril. 2006. PMID: 16818035

3

Chromosomal fragile sites in schizophrenic patients.

Demirhan O, Tastemir D, Sertdemir Y. Demirhan O, et al. Among authors: tastemir d. Genetika. 2006 Jul;42(7):985-92. Genetika. 2006. PMID: 16915931

4

Chromosome aberrations in a schizophrenia population.

Demirhan O, Taştemir D. Demirhan O, et al. Among authors: tastemir d. Schizophr Res. 2003 Dec 1;65(1):1-7. doi: 10.1016/s0920-9964(02)00504-2. Schizophr Res. 2003. PMID: 14623367

5

Cytogenetic effects of ethanol on chronic alcohol users.

Demirhan O, Tastemir D. Demirhan O, et al. Among authors: tastemir d. Alcohol Alcohol. 2008 Mar-Apr;43(2):127-36. doi: 10.1093/alcalc/agm155. Epub 2008 Jan 18. Alcohol Alcohol. 2008. PMID: 18204049

6

The expression of folate sensitive fragile sites in patients with bipolar disorder.

Demirhan O, Tastemir D, Sertdemir Y. Demirhan O, et al. Among authors: tastemir d. Yonsei Med J. 2009 Feb 28;50(1):137-41. doi: 10.3349/ymj.2009.50.1.137. Epub 2008 Feb 24. Yonsei Med J. 2009. PMID: 19259360 Free PMC article.

7

Cytogenetic study of recurrent miscarriages and their parents.

Tunç E, Demirhan O, Demir C, Tastemir D. Tunç E, et al. Among authors: tastemir d. Genetika. 2007 Apr;43(4):545-52. Genetika. 2007. PMID: 17555132 Clinical Trial.

8

Chromosomal fragile site expression in Turkish psychiatric patients.

Taştemir D, Demirhan O, Sertdemir Y. Taştemir D, et al. Psychiatry Res. 2006 Nov 15;144(2-3):197-203. doi: 10.1016/j.psychres.2005.02.010. Epub 2006 Sep 26. Psychiatry Res. 2006. PMID: 17007939

9

Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.

Pazarbaşi A, Demirhan O, Turgut M, Güzel I, Taştemir D. Pazarbaşi A, et al. Among authors: tastemir d. Genet Couns. 2008;19(3):301-8. Genet Couns. 2008. PMID: 18990986

10

A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome.

Demirhan O, Taştemir D, Diler RS, Firat S, Avci A. Demirhan O, et al. Among authors: tastemir d. Yonsei Med J. 2003 Aug 30;44(4):583-92. doi: 10.3349/ymj.2003.44.4.583. Yonsei Med J. 2003. PMID: 12950112 Free article.

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