A. Hatzaki

发表

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

D. Yannoukakos, J. Economides, K. Brøndum‐Nielsen, 2002, International journal of pediatric otorhinolaryngology.

Endothelial nitric oxide synthase gene polymorphisms in recurrent spontaneous abortions

K. Lamnissou, E. Tsaliki, L. Florentin-Arar, 2008, Archives of Gynecology and Obstetrics.

Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.

M. Petersen, M. Grigoriadou, T. Antoniadi, 2010, Genetic testing and molecular biomarkers.

Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.

C. Kanaka-Gantenbein, V. Velissariou, S. Christopoulou, 2006, European journal of medical genetics.

Genetic skeletal disorders of the fetus and infant: pathologic and molecular findings in a series of 41 cases.

A. Karantanas, E. Patsouris, A. Konstantinidou, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Identification of an alleged offender of murder by VNTR analysis: case report.

A. Koutselinis, A. Hatzaki, M. Georgiou, 2000, The American journal of forensic medicine and pathology.

A study of five variable number tandem repeat (VNTR) loci in the Greek population.

D. Loukopoulos, H. Spiliopoulou, A. Koutselinis, 1995, Molecular and cellular probes.

The Replacement of Cytogenetic Analysis by Direct Chorionic Villi Sampling Preparation with Quantitative Fluorescence PCR

S. Sifakis, V. Velissariou, G. Christopoulou, 2009, Gynecologic and Obstetric Investigation.

Genetic Analysis of Syndromic and Nonsyndromic Patients With Craniosynostosis Identifies Novel Mutations in the TWIST1 and EFNB1 Genes

P. Kollia, V. Aleporou, A. Hatzaki, 2018, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Prenatal diagnosis of achondroplasia presenting with multiple‐suture synostosis: a novel association

V. Velissariou, T. Antoniadi, C. Karadimas, 2006, Prenatal diagnosis.

A. Konstantinidou, S. Sifakis, V. Velissariou, 2011, American journal of medical genetics. Part A.

A Novel de Novo Mutation Within EFNB1 Gene in a Young Girl with Craniofrontonasal Syndrome

P. Kollia, V. Aleporou, A. Hatzaki, 2012, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.

C. Sismani, P. Patsalis, C. Bartsocas, 2007, European journal of medical genetics.

A modified mutagenic PCR-RFLP method for K-ras codon 12 and 13 mutations detection in NSCLC patients.

K. Anagnostopoulou, P. Kosmidis, M. Mihalatos, 2001, Molecular and cellular probes.

Prenatal diagnosis of hypochondroplasia: Report of two cases

S. Sifakis, G. Nasioulas, V. Velissariou, 2006, American journal of medical genetics. Part A.

The implications of using mutagenic primers in combination with Taq polymerase having proofreading activity.

G. Nasioulas, V. Metaxa-Mariatou, E. Papadopoulou, 2004, Biologicals : journal of the International Association of Biological Standardization.

The impact of heterozygosity for the factor V Leiden and factor II G20210A mutations on the risk of thrombosis in Greek patients.

G. Nasioulas, V. Metaxa-Mariatou, P. Philalithis, 2003, International angiology : a journal of the International Union of Angiology.

A. Konstantinidou, S. Sifakis, V. Velissariou, 2011, American journal of medical genetics. Part A.