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Results:
1-17
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Results: 17
Authors:
Catassi, C
Cellier, C
Cerf-Bensussan, N
Ciclitira, PJ
Collin, P
Corazza, GR
Dickey, W
Fasano, A
Holmes, GKT
Klincewicz, P
Mearin, ML
Mulder, CJJ
Murray, JA
Pena, AS
Schuppan, D
Sollid, LM
Uil, JJ
Wahab, PJ
Walker-Smith, JA
Watson, P
Van Belzen, M
Von Blomberg, BME
Bouquet, J
Bijleveldt, CMA
Crusius, JBA
Douwes, AC
George, EK
Hamer, RJ
Janssen, FW
Meyer, JWR
Sinaasappel, M
Rostami, K
Taminiau, JAJM
Vader, LW
Wijmenga, C
Citation: C. Catassi et al., When is a coeliac a coeliac? Report of a working group of the United European Gastroenterology Week in Amsterdam, 2001, EUR J GASTR, 13(9), 2001, pp. 1123-1128
Authors:
van de Sluis, B
Nanji, MS
Breen, M
Pearson, PL
Oost, BA
Cox, DW
Wijmenga, C
Citation: B. Van De Sluis et al., Characterization and chromosomal localization of five canine ATOX1 pseudogenes, CYTOG C GEN, 93(1-2), 2001, pp. 105-108
Authors:
van Tilburg, J
van Haeften, TW
Pearson, P
Wijmenga, C
Citation: J. Van Tilburg et al., Defining the genetic contribution of type 2 diabetes mellitus, J MED GENET, 38(9), 2001, pp. 569-578
Authors:
Ausems, MGEM
ten Berg, K
Sandkuijl, LA
Kroos, MA
Bardoel, AFJ
Roumelioti, KN
Reuser, AJJ
Sinke, R
Wijmenga, C
Citation: Mgem. Ausems et al., Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations, J MED GENET, 38(8), 2001, pp. 527-529
Authors:
Papadopoulos, GK
Wijmenga, C
Koning, F
Citation: Gk. Papadopoulos et al., Interplay between genetics and the environment in the development of celiac disease: perspectives for a healthy life, J CLIN INV, 108(9), 2001, pp. 1261-1266
Authors:
Wijmenga, C
Hansen, RS
Gimelli, G
Bjorck, EJ
Davies, EG
Valentine, D
Belohradsky, BH
van Dongen, JJ
Smeets, DFCM
van den Heuvel, LPWJ
Luyten, JAFM
Strengman, E
Weemaes, C
Pearson, PL
Citation: C. Wijmenga et al., Genetic variation in ICF syndrome: Evidence for genetic heterogeneity, HUM MUTAT, 16(6), 2000, pp. 509-517
Authors:
Hansen, RS
Stoger, R
Wijmenga, C
Stanek, AM
Canfield, TK
Luo, P
Matarazzo, MR
D'Esposito, M
Feil, R
Gimelli, G
Weemaes, CMR
Laird, CD
Gartler, SM
Citation: Rs. Hansen et al., Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant, HUM MOL GEN, 9(18), 2000, pp. 2575-2587
Authors:
van de Sluis, B
Kole, S
van Wolferen, M
Holmes, NG
Pearson, PL
Rothuizen, J
van Oost, BA
Wijmenga, C
Citation: B. Van De Sluis et al., Refined genetic and comparative physical mapping of the canine copper toxicosis locus, MAMM GENOME, 11(6), 2000, pp. 455-460
Authors:
Bjorck, EJ
Bui, TH
Wijmenga, C
Grandell, U
Nordenskjold, M
Citation: Ej. Bjorck et al., Early prenatal diagnosis of the ICF syndrome, PRENAT DIAG, 20(10), 2000, pp. 828-831
Authors:
Muller, T
Wijmenga, C
Phillips, AD
Janecke, A
Houwen, RHJ
Fischer, H
Ellemunter, H
Fruhwirth, M
Offner, F
Hofer, S
Muller, W
Booth, IW
Heinz-Erian, P
Citation: T. Muller et al., Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes, GASTROENTY, 119(6), 2000, pp. 1506-1513
Authors:
van Tilburg, JHO
Rozeman, LB
van Someren, H
Rigters-Aris, CAE
Freriks, JP
Pearson, PL
Sandkuijl, LA
van Haeften, TW
Wijmenga, C
Citation: Jho. Van Tilburg et al., The exon 16-3t variant of the sulphonylurea receptor gene is not a risk factor for Type II diabetes mellitus in the Dutch Breda cohort, DIABETOLOG, 43(5), 2000, pp. 681-682
Authors:
van de Sluis, BJA
Breen, M
Nanji, M
van Wolferen, M
de Jong, P
Binns, MM
Pearson, PL
Kuipers, J
Rothuizen, J
Cox, DW
Wijmenga, C
van Oost, BA
Citation: Bja. Van De Sluis et al., Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16, HUM MOL GEN, 8(3), 1999, pp. 501-507
Authors:
van der Reijden, BA
Dauwerse, HG
Giles, RH
Jagmohan-Changur, S
Wijmenga, C
Liu, PP
Smit, B
Wessels, HW
Beverstock, GC
Jotterand-Bellomo, M
Martinet, D
Muhlematter, D
Lafage-Pochitaloff, M
Gabert, J
Reiffers, J
Bilhou-Nabera, C
van Ommen, GJB
Hagemeijer, A
Breuning, MH
Citation: Ba. Van Der Reijden et al., Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered, ONCOGENE, 18(2), 1999, pp. 543-550
Authors:
Scheres, JMJC
de Pater, JM
Stoutenbeek, P
Wijmenga, C
Rosenberg, C
Pearson, PL
Citation: Jmjc. Scheres et al., Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas - Possible trisomic or tetrasomic zygote rescue in fetal teratoma with anadditional isochromosome 1q, CANC GENET, 115(1), 1999, pp. 1-10
Authors:
Bank, RA
Robins, SP
Wijmenga, C
Breslau-Siderius, LJ
Bardoel, AFJ
Van der Sluijs, HA
Pruijs, HEH
TeKoppele, JM
Citation: Ra. Bank et al., Defective collagen crosslinking in bone, but not in ligament or cartilage,in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17, P NAS US, 96(3), 1999, pp. 1054-1058
Authors:
Hansen, RS
Wijmenga, C
Luo, P
Stanek, AM
Canfield, TK
Weemaes, CMR
Gartler, SM
Citation: Rs. Hansen et al., The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome, P NAS US, 96(25), 1999, pp. 14412-14417
Authors:
Wijmenga, C
Muller, T
Murli, IS
Brunt, T
Feichtinger, H
Schonitzer, D
Houwen, RHJ
Muller, W
Sandkuijl, LA
Pearson, PL
Citation: C. Wijmenga et al., Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson'sdisease, EUR J HUM G, 6(6), 1998, pp. 624-628
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1-17
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