Sofocleous C - Search Results

1

10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.

Sofocleous C, Kitsiou S, Fryssira H, Kolialexi A, Kalaitzidaki M, Roma E, Tsangaris GT, Chistofidou C, Metaxotou C, Kanavakis E, Mavrou A. Sofocleous C, et al. In Vivo. 2008 Jul-Aug;22(4):451-5. In Vivo. 2008. PMID: 18712171 Free article.

2

Identification of three polymorphisms in the dystrophin gene.

Kekou K, Mavrou A, Sofocleous C, Metaxotou C. Kekou K, et al. Among authors: sofocleous c. Mol Cell Probes. 1999 Dec;13(6):453-4. doi: 10.1006/mcpr.1999.0272. Mol Cell Probes. 1999. PMID: 10657151

3

Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.

Vrettou C, Traeger-Synodinos J, Tzetis M, Palmer G, Sofocleous C, Kanavakis E. Vrettou C, et al. Among authors: sofocleous c. Hum Mutat. 2004 May;23(5):513-21. doi: 10.1002/humu.20022. Hum Mutat. 2004. PMID: 15108284

4

Non-Hodgkin lymphoma in a child with Williams syndrome.

Amenta S, Moschovi M, Sofocleous C, Kostaridou S, Mavrou A, Fryssira H. Amenta S, et al. Among authors: sofocleous c. Cancer Genet Cytogenet. 2004 Oct 1;154(1):86-8. doi: 10.1016/j.cancergencyto.2004.02.004. Cancer Genet Cytogenet. 2004. PMID: 15381380

5

Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population.

Amenta S, Sofocleous C, Kolialexi A, Thomaidis L, Giouroukos S, Karavitakis E, Mavrou A, Kitsiou S, Kanavakis E, Fryssira H. Amenta S, et al. Among authors: sofocleous c. Pediatr Res. 2005 Jun;57(6):789-95. doi: 10.1203/01.PDR.0000157675.06850.68. Epub 2005 Mar 17. Pediatr Res. 2005. PMID: 15774842

6

Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).

Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A. Kolialexi A, et al. Among authors: sofocleous c. In Vivo. 2006 Jul-Aug;20(4):473-8. In Vivo. 2006. PMID: 16900777 Free article.

7

Juvenile idiopathic arthritis-type disease associated with chromosomal aberrations.

Salavoura K, Dracou C, Kolialexi A, Drakonaki S, Sofocleous C, Mavrou A. Salavoura K, et al. Among authors: sofocleous c. Clin Exp Rheumatol. 2008 Mar-Apr;26(2):347-50. Clin Exp Rheumatol. 2008. PMID: 18565261

8

Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome.

Salavoura K, Kolialexi A, Sofocleous C, Kalaitzidaki M, Pampanos A, Kitsiou S, Mavrou A. Salavoura K, et al. Among authors: sofocleous c. Genet Couns. 2008;19(2):219-24. Genet Couns. 2008. PMID: 18618997

9

Molecular diagnosis of Fragile X syndrome.

Sofocleous C, Kolialexi A, Mavrou A. Sofocleous C, et al. Expert Rev Mol Diagn. 2009 Jan;9(1):23-30. doi: 10.1586/14737159.9.1.23. Expert Rev Mol Diagn. 2009. PMID: 19099346

10

PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol.

Christofidou C, Sofocleous C, Vrettou C, Destouni A, Traeger-Synodinos J, Kekou K, Palmer G, Kokkali G, Mavrou A, Kitsiou S, Kanavakis E. Christofidou C, et al. Among authors: sofocleous c. Reprod Biomed Online. 2009 Sep;19(3):418-25. doi: 10.1016/s1472-6483(10)60178-2. Reprod Biomed Online. 2009. PMID: 19778490

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