Tunçbilek E - Search Results

1

Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.

Utine GE, Aktas D, Boduroğlu K, Alikasifoğlu M, Tunçbilek E. Utine GE, et al. Among authors: tuncbilek e. Genet Couns. 2007;18(2):171-7. Genet Couns. 2007. PMID: 17710869

2

Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study.

Aktas D, Tuncbilek E. Aktas D, et al. Among authors: tuncbilek e. Cancer Genet Cytogenet. 2006 Nov;171(1):72-5. doi: 10.1016/j.cancergencyto.2006.06.010. Cancer Genet Cytogenet. 2006. PMID: 17074595

3

Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH.

Utine EG, Alanay Y, Aktas D, Alikasifoglu M, Boduroglu K, Vermeesch J, Tuncbilek E, Fryns JP. Utine EG, et al. Among authors: tuncbilek e. Eur J Med Genet. 2008 Jul-Aug;51(4):343-50. doi: 10.1016/j.ejmg.2008.03.002. Epub 2008 Mar 27. Eur J Med Genet. 2008. PMID: 18440888

4

Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients.

Utine GE, Celik T, Alanay Y, Alikaşifoğlu M, Boduroğlu K, Tunçbilek E, Aktaş D. Utine GE, et al. Among authors: tuncbilek e. Turk J Pediatr. 2009 May-Jun;51(3):199-206. Turk J Pediatr. 2009. PMID: 19817261

5

Myelodysplastic syndrome associated with monosomy 7 in a child with Bloom syndrome.

Aktas D, Koc A, Boduroglu K, Hicsonmez G, Tuncbilek E. Aktas D, et al. Among authors: tuncbilek e. Cancer Genet Cytogenet. 2000 Jan 1;116(1):44-6. doi: 10.1016/s0165-4608(99)00099-0. Cancer Genet Cytogenet. 2000. PMID: 10616531

6

Screening for the fragile X syndrome among mentally retarded males by hair root analysis.

Tunçbilek E, Alikasifoğlu M, Aktas D, Duman F, Yanik H, Anar B, Oostra B, Willemsen R. Tunçbilek E, et al. Am J Med Genet. 2000 Nov 13;95(2):105-7. doi: 10.1002/1096-8628(20001113)95:2<105::aid-ajmg3>3.0.co;2-6. Am J Med Genet. 2000. PMID: 11078558

7

Kabuki syndrome and trisomy 10p.

Utine GE, Alanay Y, Atkaş D, Boduroğlu K, Alikaşifoğlu M, Tunçbilek E. Utine GE, et al. Among authors: tuncbilek e. Genet Couns. 2008;19(3):291-300. Genet Couns. 2008. PMID: 18990985

8

Opinions of Turkish physicians towards termination of pregnancy for fetal disorders.

Utine GE, Kiper PO, Salanci BV, Alanay Y, Aktaş D, Alikaşifoğlu M, Boduroğlu K, Tunçbilek E. Utine GE, et al. Among authors: tuncbilek e. Genet Couns. 2011;22(4):401-9. Genet Couns. 2011. PMID: 22303801

9

Ipsilateral foot and contralateral hand anomalies in a patient with Poland-Moebius syndrome.

Cetin II, Aktaş D, Tunçbilek E. Cetin II, et al. Among authors: tuncbilek e. Eur J Med Genet. 2005 Apr-Jun;48(2):183-7. doi: 10.1016/j.ejmg.2005.01.022. Epub 2005 Feb 1. Eur J Med Genet. 2005. PMID: 16053910

10

Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogue.

Utine GE, Alikasifoglu A, Alikasifoglu M, Tuncbilek E. Utine GE, et al. Among authors: tuncbilek e. Eur J Med Genet. 2006 Jan-Feb;49(1):79-82. doi: 10.1016/j.ejmg.2005.04.020. Epub 2005 Jun 29. Eur J Med Genet. 2006. PMID: 16473313

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