TRIANGULAR FINITE ELEMENTS FOR POISSON'S EQUATION WITH NODALS DERIVATIVES. = ELEMENTS FINIS TRIANGULAIRES POUR L'EQUATION DE POISSON AVEC DES DERIVEES NODALESTSIPOURAS P.1976; COMPUTERS AND STRUCT.; G.B.; DA. 1976; VOL. 6; NO 3; PP. 173-176; BIBL. 1 REF.Article

COMPACT REPRESENTATION OF TRIANGULAR FINITE ELEMENTS FOR POISSON'S EQUATION.TSIPOURAS P.1977; INTERNATION. J. NUMER. METHODS ENGNG; U.S.A.; DA. 1977; VOL. 11; NO 3; PP. 419-430; BIBL. 4 REF.Article

NUMERICAL STABILITY OF INCOMPLETELY INTEGRATED SHAPE FUNCTIONS.TSIPOURAS P.1977; COMPUTERS AND STRUCT.,; G.B.; DA. 1977; VOL. 7; NO 5; PP. 679-680; BIBL. 4 REF.Article

Marfan syndrome: light at the end of the tunnel?TSIPOURAS, P.American journal of human genetics. 1990, Vol 46, Num 4, pp 643-645, issn 0002-9297, 3 p.Article

A MODEL FOR ESTIMATING PERSISTENCE PROBABILITIESLUND IA; TSIPOURAS P.1982; JOURNAL OF APPLIED METEOROLOGY; ISSN 0021-8952; USA; DA. 1982; VOL. 21; NO 7; PP. 988-994; BIBL. 5 REF.Article

Oral findings in osteogenesis imperfectaSCHWARTZ, S; TSIPOURAS, P.Oral surgery, oral medicine, oral pathology. 1984, Vol 57, Num 2, pp 161-167, issn 0030-4220Article

Genetic disorders of collagenTSIPOURAS, P; RAMIREZ, F.Journal of medical genetics. 1987, Vol 24, Num 1, pp 2-8, issn 0022-2593Article

Osteogenesis imperfecta type IV: biochemical confirmation of genetic linkage to the proα2(1) gene of type I collagenWENSTRUP, R. J; TSIPOURAS, P; BYERS, P. H et al.The Journal of clinical investigation. 1986, Vol 78, Num 6, pp 1449-1455, issn 0021-9738Article

Linkage disequilibrium between two restriction sites in the COL2AI geneSCHWARTZ, R. C; SARFARAZI, M; TSIPOURAS, P et al.American journal of human genetics. 1990, Vol 46, Num 6, pp 1214-1215, issn 0002-9297, 2 p.Article

Increased aortic root stiffness associated with osteogenesis imperfectaKALATH, S; TSIPOURAS, P; SILVER, F. H et al.Annals of biomedical engineering. 1987, Vol 15, Num 1, pp 91-99, issn 0090-6964Article

Neurologic correlates of osteogenesis imperfectaTSIPOURAS, P; BARABAS, G; MATTHEWS, W. S et al.Archives of neurology (Chicago). 1986, Vol 43, Num 2, pp 150-152, issn 0003-9942Article

Non-invasive assessment of aortic mechanical propertiesSATISH KALATH; TSIPOURAS, P; SILVER, F. H et al.Annals of biomedical engineering. 1986, Vol 14, Num 6, pp 513-524, issn 0090-6964Article

GENETIC STRUCTURE OF THE GREEK GYPSIESBARTSOCAS CS; KARAYANNI C; TSIPOURAS P et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 1; PP. 5-10; BIBL. 33 REF.Article

A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasiaSTOILOV, I; KILPATRICK, M. W; TSIPOURAS, P et al.American journal of medical genetics. 1995, Vol 55, Num 1, pp 127-133, issn 0148-7299Article

Two RFLPs in the 5' end of the human osteonectin (ON) geneSCHWARTZ, R. C; YOUNG, M. F; TSIPOURAS, P et al.Nucleic acids research. 1988, Vol 16, Num 18, issn 0305-1048, 9076 [1p.]Article

An RFLP in the gene for the human pro-alpha 2 chain of type V collagen (COL5A2)SCHWARTZ, R. C; LIDDELL, A; RAMIREZ, F et al.Nucleic acids research. 1988, Vol 16, Num 11, issn 0305-1048, 5225Article

Restriction fragment length polymorphism associated with the proα2(I) gene of human type I procollagen: application to a family with an autosomal dominant form of osteogenesis imperfectaTSIPOURAS, P; MYERS, J. C; RAMIREZ, F et al.The Journal of clinical investigation. 1983, Vol 72, Num 4, pp 1262-1267, issn 0021-9738Article

Marfan syndrome is closely linked to a marker on chromosome 15q1.5→q2.1TSIPOURAS, P; SARFARAZI, M; DEVI, A et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 10, pp 4486-4488, issn 0027-8424, 3 p.Article

Split hand foot malformation is associated with a reduced level of Dactylin gene expressionBASEL, D; DEPAEPE, A; KILPATRICK, M. W et al.Clinical genetics. 2003, Vol 64, Num 4, pp 350-354, issn 0009-9163, 5 p.Article

Use of molecular haplotypes specific for the human pro α2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfectaFALK, C. T; SCHWARTZ, R. C; RAMIREZ, F et al.American journal of human genetics. 1986, Vol 38, Num 3, pp 269-279, issn 0002-9297Article

Orthopaedic manifestations of Ehlers-Danlos SyndromeSTANITSKI, D. F; NADJARIAN, R; STANITSKI, C. L et al.Clinical orthopaedics and related research. 2000, Num 376, pp 213-221, issn 0009-921XArticle

Ehlers-Danlos syndromes : Revised nosology, Villefranche, 1997BEIGHTON, P; DE PAEPE, A; STEINMANN, B et al.American journal of medical genetics. 1998, Vol 77, Num 1, pp 31-37, issn 0148-7299Article

Spondyloepiphyseal dysplasia congenita : genetic linkage to type II collagen (COL2AI)ANDERSON, I. J; GOLDBERG, R. B; MARION, R. W et al.American journal of human genetics. 1990, Vol 46, Num 5, pp 896-901, issn 0002-9297, 6 p.Article

Chronic pain is a manifestation of the Ehlers-Danlos syndromeSACHETI, A; SZEMERE, J; BERNSTEIN, B et al.Journal of pain and symptom management. 1997, Vol 14, Num 2, pp 88-93, issn 0885-3924Article

Mild spondyloepiphyseal dysplasia (Namaqualand type) : genetic linkage to the type II collagen gene (COL2AI)SHER, C; RAMESAR, R; MARTELL, R et al.American journal of human genetics. 1991, Vol 48, Num 3, pp 518-524, issn 0002-9297Article