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Results: 1-25 | 26-27
Results: 1-25/27
Investigation of a cluster of children with Down Syndrome born to mothers who had attended a school in Dundalk, Ireland. (vol 57, pg 793, 2000)
Authors: Dean, G Nevin, NC Mikkelsen, M Karadima, G Petersen, MB Kelly, M O'Sullivan, J
Citation: G. Dean et al., Investigation of a cluster of children with Down Syndrome born to mothers who had attended a school in Dundalk, Ireland. (vol 57, pg 793, 2000), OCC ENVIR M, 58(5), 2001, pp. 353-353
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome
Authors: Hertz, JM Juncker, I Persson, U Matthijs, G Schmidtke, J Petersen, MB Kjeldsen, M Gregersen, N
Citation: Jm. Hertz et al., Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome, HUM MUTAT, 18(2), 2001, pp. 141-148
Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree
Authors: Kitsos, G Eiberg, H Economou-Petersen, E Wirtz, MK Kramer, PL Aspiotis, M Tommerup, N Petersen, MB Psilas, K
Citation: G. Kitsos et al., Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree, EUR J HUM G, 9(6), 2001, pp. 452-457
Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis
Authors: Velissariou, V Antoniadi, T Patsalis, P Christopoulou, S Hatzipouliou, A Donoghue, J Bakou, K Kaminopetros, P Athanassiou, V Petersen, MB
Citation: V. Velissariou et al., Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis, PRENAT DIAG, 21(6), 2001, pp. 484-487
Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation
Authors: Antoniadi, T Pampanos, A Petersen, MB
Citation: T. Antoniadi et al., Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation, PRENAT DIAG, 21(1), 2001, pp. 10-13
Scratch induction in the rat by intradermal serotonin: a model for pruritus
Authors: Thomsen, JS Petersen, MB Benfeldt, E Jensen, SB Serup, J
Citation: Js. Thomsen et al., Scratch induction in the rat by intradermal serotonin: a model for pruritus, ACT DER-VEN, 81(4), 2001, pp. 250-254
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland
Authors: Dean, G Nevin, NC Mikkelsen, M Karadima, G Petersen, MB Kelly, M O'Sullivan, J
Citation: G. Dean et al., Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland, OCC ENVIR M, 57(12), 2000, pp. 793-804
Patterns of meiotic recombination on the long arm of human chromosome 21
Authors: Lynn, A Kashuk, C Petersen, MB Bailey, JA Cox, DR Antonarakis, SE Chakravarti, A
Citation: A. Lynn et al., Patterns of meiotic recombination on the long arm of human chromosome 21, GENOME RES, 10(9), 2000, pp. 1319-1332
Mutation analysis of the GJB2 (Connexin 26) gene by DGGE in Greek patientswith sensorineural deafness
Authors: Antoniadi, T Gronskov, K Sand, A Pampanos, A Brondum-Nielsen, K Petersen, MB
Citation: T. Antoniadi et al., Mutation analysis of the GJB2 (Connexin 26) gene by DGGE in Greek patientswith sensorineural deafness, HUM MUTAT, 16(1), 2000, pp. 7-12
Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis
Authors: Panas, M Karadima, G Kalfakis, N Psarrou, O Floroskoufi, P Kladi, A Petersen, MB Vassilopoulos, D
Citation: M. Panas et al., Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis, J NEUROL, 247(12), 2000, pp. 940-942
Use of a migration assay for the separation of adult pyrantel-susceptible and -resistant Oesophagostomum dentatum
Authors: Petersen, MB Craven, J Bjorn, H Nansen, P
Citation: Mb. Petersen et al., Use of a migration assay for the separation of adult pyrantel-susceptible and -resistant Oesophagostomum dentatum, VET PARASIT, 91(1-2), 2000, pp. 141-145
Nondisjunction in trisomy 21: Origin and mechanisms
Authors: Petersen, MB Mikkelsen, M
Citation: Mb. Petersen et M. Mikkelsen, Nondisjunction in trisomy 21: Origin and mechanisms, CYTOG C GEN, 91(1-4), 2000, pp. 199-203
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome
Authors: Petersen, MB Karadima, G Samaritaki, M Avramopoulos, D Vassilopoulos, D Mikkelsen, M
Citation: Mb. Petersen et al., Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome, AM J MED G, 93(5), 2000, pp. 366-372
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases
Authors: Tsezou, A Kitsiou, S Galla, A Petersen, MB Karadima, G Syrrou, M Sahlen, S Blennow, E
Citation: A. Tsezou et al., Molecular cytogenetic characterization and origin of two de novo duplication 9p cases, AM J MED G, 91(2), 2000, pp. 102-106
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype
Authors: Barbi, G Kennerknecht, I Wohr, G Avramopoulos, D Karadima, G Petersen, MB
Citation: G. Barbi et al., Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype, AM J MED G, 91(2), 2000, pp. 116-122
Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation
Authors: Pampanos, A Neou, P Iliades, T Apostolopoulos, N Voyiatzis, N Grigoriadou, M Katsichti, L Skevas, A Petersen, MB
Citation: A. Pampanos et al., Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation, CLIN GENET, 57(3), 2000, pp. 232-234
Pharmacokinetics of fenbendazole following intravenous and oral administration to pigs
Authors: Petersen, MB Friis, C
Citation: Mb. Petersen et C. Friis, Pharmacokinetics of fenbendazole following intravenous and oral administration to pigs, AM J VET RE, 61(5), 2000, pp. 573-576
The influence of storage on aroma, soluble solids, acid and colour of sourcherries (Prunus cerasus L.) cv. Stevnsbaer
Authors: Petersen, MB Poll, L
Citation: Mb. Petersen et L. Poll, The influence of storage on aroma, soluble solids, acid and colour of sourcherries (Prunus cerasus L.) cv. Stevnsbaer, EUR FOOD RE, 209(3-4), 1999, pp. 251-256
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors
Authors: Antoniadi, T Hatzis, T Kroupis, C Economou-Petersen, E Petersen, MB
Citation: T. Antoniadi et al., Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors, AM J HEMAT, 61(4), 1999, pp. 265-267
Apolipoprotein E and presenilin-1 genotypes in Huntington's disease
Authors: Panas, M Avramopoulos, D Karadima, G Petersen, MB Vassilopoulos, D
Citation: M. Panas et al., Apolipoprotein E and presenilin-1 genotypes in Huntington's disease, J NEUROL, 246(7), 1999, pp. 574-577
Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affectingclinical outcome
Authors: Wang, MS Schinzel, A Kotzot, D Balmer, D Casey, R Chodirker, BN Gyftodimou, J Petersen, MB Lopez-Rangel, E Robinson, WP
Citation: Ms. Wang et al., Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affectingclinical outcome, AM J MED G, 86(1), 1999, pp. 34-43
Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in aboy with a ring chromosome 18: additional evidence of autoimmunity or IDDMgene(s) on chromosome 18
Authors: Dacou-Voutetakis, C Sertedaki, A Maniatis-Christidis, M Sarri, C Karadima, G Petersen, MB Xaidara, A Kanariou, M Nicolaidou, P
Citation: C. Dacou-voutetakis et al., Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in aboy with a ring chromosome 18: additional evidence of autoimmunity or IDDMgene(s) on chromosome 18, J MED GENET, 36(2), 1999, pp. 156-158
The hemispherical Harris-Galante acetabular cup, inserted without cement -The results of an eight to eleven-year follow-up of one hundred and sixty-eight hips
Authors: Petersen, MB Poulsen, IH Thomsen, J Solgaard, S
Citation: Mb. Petersen et al., The hemispherical Harris-Galante acetabular cup, inserted without cement -The results of an eight to eleven-year follow-up of one hundred and sixty-eight hips, J BONE-AM V, 81A(2), 1999, pp. 219-224
Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction
Authors: Gyftodimou, J Karadima, G Pandelia, E Vassilopoulos, D Petersen, MB
Citation: J. Gyftodimou et al., Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction, CLIN GENET, 55(6), 1999, pp. 483-486
High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness
Authors: Antoniadi, T Rabionet, R Kroupis, C Aperis, GA Economides, J Petmezakis, J Economou-Petersen, E Estivill, X Petersen, MB
Citation: T. Antoniadi et al., High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness, CLIN GENET, 55(5), 1999, pp. 381-382
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