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Results: 10

Authors: SYRROU M PATSALIS PC GEORGIOU I HADJIMARCOU MI CONSTANTINOUDELTAS CD PAGOULATOS G
Citation: M. Syrrou et al., EVIDENCE FOR HIGH-RISK HAPLOTYPES AND (CGG)N EXPANSION IN FRAGILE-X SYNDROME IN THE HELLENIC POPULATION OF GREECE AND CYPRUS (VOL 64, PG 234, 1996), American journal of medical genetics, 64(3), 1996, pp. 527-527

Authors: SYRROU M PATSALIS PC GEORGIOU I HADJIMARCOU MI CONSTANTINOUDELTAS CD PAGOULATOS G
Citation: M. Syrrou et al., EVIDENCE FOR HIGH-RISK HAPLOTYPES AND (CGG)N EXPANSION IN FRAGILE-X SYNDROME IN THE HELLENIC POPULATION OF GREECE AND CYPRUS, American journal of medical genetics, 64(1), 1996, pp. 234-238

Authors: CONSTANTINOUDELTAS CD PAPAGEORGIOU E BOTEVA K CHRISTODOULOU K BREUNING MH PETERS DJM PIERIDES A
Citation: Cd. Constantinoudeltas et al., GENETIC-HETEROGENEITY IN ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE IN CYPRIOT FAMILIES, Human genetics, 95(4), 1995, pp. 416-423

Authors: CONSTANTINOUDELTAS CD PIERIDES A
Citation: Cd. Constantinoudeltas et A. Pierides, PRESYMPTOMATIC MOLECULAR DIAGNOSIS OF ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE USING PKD1 AND PKD2-LINKED MARKERS, American journal of human genetics, 57(4), 1995, pp. 1909-1909

Authors: ANGELICHEVA D BOTEVA K JORDANOVA A SAVOV A KUFARDJIEVA A TOLUN A TELATAR M AKARSUBASI A KOPRUBASI F AYDOGDU S DEMIRKOL M KURDOGLU G CONSTANTINOUDELTAS CD GEORGIOU C DEAN M IVASCHENKO T BARANOV V KALAYDJIEVA L
Citation: D. Angelicheva et al., CYSTIC-FIBROSIS PATIENTS FROM THE BLACK-SEA REGION - THE 1677DELTA MUTATION, Human mutation, 3(4), 1994, pp. 353-357

Authors: SPOTILA LD COLIGE A SEREDA L CONSTANTINOUDELTAS CD WHYTE MP RIGGS BL SHAKER JL SPECTOR TD HUME E OLSEN N ATTIE M TENENHOUSE A SHANE E BRINEY W PROCKOP DJ
Citation: Ld. Spotila et al., MUTATION ANALYSIS OF CODING SEQUENCES FOR TYPE-I PROCOLLAGEN IN INDIVIDUALS WITH LOW BONE-DENSITY, Journal of bone and mineral research, 9(6), 1994, pp. 923-932

Authors: MOTTES M SANGALLI A VALLI M FORLINO A GOMEZLIRA M ANTONIAZZI F CONSTANTINOUDELTAS CD CETTA G PIGNATTI PF
Citation: M. Mottes et al., A BASE SUBSTITUTION AT IVS-19 3'-END SPLICE JUNCTION CAUSES EXON-20 SKIPPING IN PRO-ALPHA-2(I) COLLAGEN MESSENGER-RNA AND PRODUCES MILD OSTEOGENESIS-IMPERFECTA, Human genetics, 93(6), 1994, pp. 681-687

Authors: BOTEVA K PAPAGEORGIOU E GEORGIOU C ANGASTINIOTIS M MIDDLETON LT CONSTANTINOUDELTAS CD
Citation: K. Boteva et al., NOVEL CYSTIC-FIBROSIS MUTATION ASSOCIATED WITH MILD DISEASE IN CYPRIOT PATIENTS, Human genetics, 93(5), 1994, pp. 529-532

Authors: PETERS DJM SPRUIT L SARIS JJ RAVINE D SANDKUIJL LA FOSSDAL R BOERSMA J VANEIJK R NORBY S CONSTANTINOUDELTAS CD PIERIDES A BRISSENDEN JE FRANTS RR VANOMMEN GJB BREUNING MH
Citation: Djm. Peters et al., CHROMOSOME 4 LOCALIZATION OF A 2ND GENE FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE, Nature genetics, 5(4), 1993, pp. 359-362

Authors: CONSTANTINOUDELTAS CD ARISTODEMOU E PANAYIDES K PIERIDES A
Citation: Cd. Constantinoudeltas et al., MOLECULAR-GENETIC STUDIES OF POLYCYSTIC KIDNEY-DISEASE IN CYPRUS REVEAL GENETIC-HETEROGENEITY AMONG FAMILIES, American journal of human genetics, 53(3), 1993, pp. 1690-1690
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