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Results:
1-17
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Results: 17
Authors:
Vink, T
Hinney, A
van Elburg, AA
van Goozen, SHM
Sandkuijl, LA
Sinke, RJ
Herpertz-Dahlmann, BM
Hebebrand, J
Remschmidt, H
van Engeland, H
Adan, RAH
Citation: T. Vink et al., Association between an agouti-related protein gene polymorphism and anorexia nervosa, MOL PSYCHI, 6(3), 2001, pp. 325-328
Authors:
Njajou, OT
Vaessen, N
Joosse, M
Berghuis, B
van Dongen, JWF
Breuning, MH
Snijders, PJLM
Rutten, WPF
Sandkuijl, LA
Oostra, BA
van Duijn, CM
Heutink, P
Citation: Ot. Njajou et al., A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis, NAT GENET, 28(3), 2001, pp. 213-214
Authors:
Galjaard, RJH
Kostakoglu, N
Hoogeboom, JJM
Breedveld, GJ
van der Linde, HC
Hovius, SER
Oostra, BA
Sandkuijl, LA
Akarsu, AN
Heutink, P
Citation: Rjh. Galjaard et al., X-linked recessive inheritance of radial ray deficiencies in a family withfour affected males, EUR J HUM G, 9(9), 2001, pp. 653-658
Authors:
Escamilla, MA
McInnes, LA
Service, SK
Spesny, M
Reus, VI
Molina, J
Gallegos, A
Fournier, E
Batki, S
Neylan, T
Matthews, C
Vinogradov, S
Roche, E
Tyler, DJ
Shimayoshi, N
Mendez, R
Ramirez, R
Ramirez, M
Araya, C
Araya, X
Leon, PE
Sandkuijl, LA
Freimer, NB
Citation: Ma. Escamilla et al., Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: A follow-up study on chromosome 18, AM J MED G, 105(2), 2001, pp. 207-213
Authors:
Terwindt, GM
Ophoff, RA
van Eijk, R
Vergouwe, MN
Haan, J
Frants, RR
Sandkuijl, LA
Ferrari, MD
Citation: Gm. Terwindt et al., Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura, NEUROLOGY, 56(8), 2001, pp. 1028-1032
Authors:
McInnes, LA
Service, SK
Reus, VI
Barnes, G
Charlat, O
Jawahar, S
Lewitzky, S
Yang, Q
Duong, QY
Spesny, M
Araya, C
Araya, X
Gallegos, A
Meza, L
Molina, J
Ramirez, R
Mendez, R
Silva, S
Fournier, E
Batki, SL
Mathews, CA
Neylan, T
Glatt, CE
Escamilla, MA
Luo, D
Gajiwala, P
Song, T
Crook, S
Nguyen, JB
Roche, E
Meyer, JM
Leon, P
Sandkuijl, LA
Freimer, NB
Chen, H
Citation: La. Mcinnes et al., Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population, P NAS US, 98(20), 2001, pp. 11485-11490
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:
van der Velden, PA
Sandkuijl, LA
Bergman, W
Pavel, S
van Mourik, L
Frants, RR
Gruis, NA
Citation: Pa. Van Der Velden et al., Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma, AM J HU GEN, 69(4), 2001, pp. 774-779
Authors:
Ophoff, RA
DeYoung, J
Service, SK
Joose, M
Caffo, NA
Sandkuijl, LA
Terwindt, GM
Haan, J
van den Maagdenberg, AMJM
Jen, J
Baloh, RW
Barilla-LaBarca, ML
Saccone, NL
Atkinson, JP
Ferrari, MD
Freimer, NB
Frants, RR
Citation: Ra. Ophoff et al., Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, AM J HU GEN, 69(2), 2001, pp. 447-453
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 der Velden, PA
Sandkuijl, LA
Bergman, W
Hille, ETM
Frants, RR
Gruis, NA
Citation: Pa. Van Der Velden et al., A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families, GENOME RES, 9(6), 1999, pp. 575-580
Authors:
Ausems, MGEM
Verbiest, J
Hermans, MMP
Kroos, MA
Beemer, FA
Wokke, JHJ
Sandkuijl, LA
Reuser, AJJ
van der Ploeg, AT
Citation: Mgem. Ausems et al., Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling, EUR J HUM G, 7(6), 1999, pp. 713-716
Authors:
Boehmer, ALM
Brinkmann, AO
Sandkuijl, LA
Halley, DJJ
Niermeijer, MF
Andersson, S
de Jong, FH
Kayserili, H
de Vroede, MA
Otten, BJ
Rouwe, CW
Mendonca, BB
Rodrigues, C
Bode, HH
de Ruiter, PE
Delemarre-van de Waal, HA
Drop, SLS
Citation: Alm. Boehmer et al., 17 beta-hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations, J CLIN END, 84(12), 1999, pp. 4713-4721
Authors:
Leegwater, PAJ
Konst, AAM
Kuyt, B
Sandkuijl, LA
Naidu, S
Oudejans, CBM
Schutgens, RBH
Pronk, JC
van der Knaap, MS
Citation: Paj. Leegwater et al., The gene for leukoencephalopathy with vanishing white matter is located onchromosome 3q27, AM J HU GEN, 65(3), 1999, pp. 728-734
Authors:
Escamilla, MA
McInnes, LA
Spesny, M
Reus, VI
Service, SK
Shimayoshi, N
Tyler, DJ
Silva, S
Molina, J
Gallegos, A
Meza, L
Cruz, ML
Batki, S
Vinogradov, S
Neylan, T
Nguyen, JB
Fournier, E
Araya, C
Barondes, SH
Leon, P
Sandkuijl, LA
Freimer, NB
Citation: Ma. Escamilla et al., Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: An initial screen for bipolar disorder loci on chromosome 18, AM J HU GEN, 64(6), 1999, pp. 1670-1678
Authors:
Service, SK
Lang, DWT
Freimer, NB
Sandkuijl, LA
Citation: Sk. Service et al., Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations, AM J HU GEN, 64(6), 1999, pp. 1728-1738
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
Risultati:
1-17
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