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A Novel de Novo Mutation Within EFNB1 Gene in a Young Girl With Craniofrontonasal SyndromeAPOSTOLOPOULOU, Despina; STRATOUDAKIS, Alexander; HATZAKI, Angeliki et al.The Cleft palate-craniofacial journal. 2012, Vol 49, Num 1, pp 109-113, issn 1055-6656, 5 p.Article

Prenatal diagnosis of achondroplasia presenting with multiple-suture synostosis : a novel associationKARADIMAS, Charalampos; TROUVAS, Dimitrios; HARITATOS, George et al.Prenatal diagnosis. 2006, Vol 26, Num 3, pp 258-261, issn 0197-3851, 4 p.Article

FGFR3 Related Skeletal Dysplasias Diagnosed Prenatally by Ultrasonography and Molecular Analysis: Presentation of 17 CasesHATZAKI, Angeliki; SIFAKIS, Stavros; THEODOROPOULOS, Perikles et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 10, pp 2426-2435, issn 1552-4825, 10 p.Article

Prevalence of GJB2 mutations in prelingual deafness in the Greek populationPAMPANOS, Andreas; ECONOMIDES, John; KONSTANTOPOULOU, Irene et al.International journal of pediatric otorhinolaryngology. 2002, Vol 65, Num 2, pp 101-108, issn 0165-5876Article

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