S. Kitsiou

发表

Two‐way trafficking of Annexin V positive cells between mother and fetus: determination of apoptosis at delivery

G. Tsangaris, E. Kanavakis, A. Mavrou, 2007, Prenatal diagnosis.

The clinical pattern of group C streptococcal pharyngitis in children

M. Moustaki, P. Nicolaidou, A. Fretzayas, 2009, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Tetrasomy 18p de novo: Parental Origin and Different Mechanisms of Formation

N. Tommerup, E. Blennow, D. Avramopoulos, 1996, European journal of human genetics : EJHG.

SMA prenatal diagnosis: a modified protocol to help differentiation between deletions and gene conversion.

C. Sofocleous, A. Mavrou, H. Fryssira, 2015, Molecular and cellular probes.

Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.

P. Vorgia, J. Traeger-Synodinos, H. Fryssira, 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Coinheritance of Noonan syndrome and Becker muscular dystrophy

A. Papadopoulou, A. Fretzayas, A. Dinopoulos, 2010, Neuromuscular Disorders.

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

E. Kanavakis, J. Traeger-Synodinos, C. Vrettou, 2009, Reproductive biomedicine online.

The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome

Xavier Estivill, Andrew J Sharp, Stefano Vicari, 2013, Genome research.

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

G. Tsangaris, C. Sofocleous, A. Mavrou, 2006, In vivo.

Long-term follow-up of a multifocal hepatic mesenchymal hamartoma producing a-fetoprotein

M. Moustaki, E. Alexopoulou, A. Fretzayas, 2009, Pediatric Surgery International.

UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis

A. Tsezou, P. Nicolaidou, A. Fretzayas, 2006, Scandinavian journal of infectious diseases.

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

G. Tsangaris, E. Kanavakis, C. Sofocleous, 2008, In vivo.

FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population

P. Patsalis, I. Georgiou, M. Petersen, 1998, Genetic epidemiology.

M. Kanariou, C. Pitsios, G. Chouliaras, 2011, European Journal of Pediatrics.

Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.

G. Tsangaris, E. Kanavakis, A. Mavrou, 2005, Anticancer research.

Clinical expression of co-inherited Dubin-Johnson and thalassaemic heterozygous states.

A. Papadopoulou, A. Fretzayas, P. Nicolaidou, 2007, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Colon Polyps in Childhood: Increased Mucosal Eosinophilia in Juvenile Polyps

J. Panayiotou, V. Syriopoulou, E. Roma-giannikou, 2009 .

Splenic granulomatous lesions in immunocompetent pediatric patients with visceral leishmaniasis.

M. Moustaki, T. Karpathios, A. Fretzayas, 2001, Scandinavian Journal of Infectious Diseases.

A case of Ehlers Danlos syndrome type VI.

A. Mavrou, A. Kolialexi, M. Valari, 2006, Genetic counseling.

Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population

A. Tsezou, M. Tzetis, E. Kanavakis, 2000, European Journal of Pediatrics.

Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.

E. Blennow, A. Tsezou, G. Karadima, 2000, American journal of medical genetics.