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                             37 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Family-Based Test for Correlation between Gene Expression and Trait Values Kraft, Peter
2003
72 5 p. 1323-1330
8 p.
artikel
2 A Genomewide Scan for Attention-Deficit/Hyperactivity Disorder in an Extended Sample: Suggestive Linkage on 17p11 Ogdie, Matthew N.
2003
72 5 p. 1268-1279
12 p.
artikel
3 A Method for the Assessment of Disease Associations with Single-Nucleotide Polymorphism Haplotypes and Environmental Variables in Case-Control Studies Zhao, Lue Ping
2003
72 5 p. 1231-1250
20 p.
artikel
4 A Multicolor FISH Assay Does Not Detect DUP25 in Control Individuals or in Reported Positive Control Cells Weiland, Yanina
2003
72 5 p. 1349-1352
4 p.
artikel
5 An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome Jaeger, E.E.M.
2003
72 5 p. 1261-1267
7 p.
artikel
6 Announcements 1 2003
72 5 p. 1355-1357
3 p.
artikel
7 Anxiety with Panic Disorder Linked to Chromosome 9q in Iceland Thorgeirsson, Thorgeir E.
2003
72 5 p. 1221-1230
10 p.
artikel
8 Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies Antoniou, A.
2003
72 5 p. 1117-1130
14 p.
artikel
9 A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q Bakker, S.C.
2003
72 5 p. 1251-1260
10 p.
artikel
10 Correction: Mitochondrial DNA Variation in Amerindians Silva Jr., Wilson A.
2003
72 5 p. 1346-1348
3 p.
artikel
11 Cost-Effective Designs for Linkage Disequilibrium Mapping of Complex Traits Service, Susan K.
2003
72 5 p. 1213-1220
8 p.
artikel
12 Down Syndrome: Visions for the 21st Century Van Dyke, Don C.
2003
72 5 p. 1354-
1 p.
artikel
13 Elevated Risk for MPNST in NF1 Microdeletion Patients De Raedt, T.
2003
72 5 p. 1288-1292
5 p.
artikel
14 Erratum 2003
72 5 p. 1358-
1 p.
artikel
15 Features of Evolution and Expansion of Modern Humans, Inferred from Genomewide Microsatellite Markers Zhivotovsky, Lev A.
2003
72 5 p. 1171-1186
16 p.
artikel
16 Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome Beales, Philip L.
2003
72 5 p. 1187-1199
13 p.
artikel
17 Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements Stankiewicz, Paweł
2003
72 5 p. 1101-1116
16 p.
artikel
18 Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V Antonellis, Anthony
2003
72 5 p. 1293-1299
7 p.
artikel
19 In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene Gicquel, Christine
2003
72 5 p. 1338-1341
4 p.
artikel
20 KLOTHO Allele Status and the Risk of Early-Onset Occult Coronary Artery Disease Arking, Dan E.
2003
72 5 p. 1154-1161
8 p.
artikel
21 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene Ofman, Rob
2003
72 5 p. 1300-1307
8 p.
artikel
22 Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an American Founder Genomic Deletion of the MSH2 Gene Wagner, Anja
2003
72 5 p. 1088-1100
13 p.
artikel
23 Molecular Cytogenetics: Protocols and Applications Li, Marilyn M.
2003
72 5 p. 1353-
1 p.
artikel
24 Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma Azzedine, H.
2003
72 5 p. 1141-1153
13 p.
artikel
25 Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 Ahmed, Zubair M.
2003
72 5 p. 1315-1322
8 p.
artikel
26 Native American Y Chromosomes in Polynesia: The Genetic Impact of the Polynesian Slave Trade Hurles, Matthew E.
2003
72 5 p. 1282-1287
6 p.
artikel
27 Past Exposure to Densely Ionizing Radiation Leaves a Unique Permanent Signature in the Genome Hande, M. Prakash
2003
72 5 p. 1162-1170
9 p.
artikel
28 Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome Heilstedt, Heidi A.
2003
72 5 p. 1200-1212
13 p.
artikel
29 Polymorphisms at the G72/G30 Gene Locus, on 13q33, Are Associated with Bipolar Disorder in Two Independent Pedigree Series * Hattori, Eiji
2003
72 5 p. 1131-1140
10 p.
artikel
30 PowerTrim: An Automated Decision Support Algorithm for Preprocessing Family-Based Genetic Data Thornton, Tricia A.
2003
72 5 p. 1280-1281
2 p.
artikel
31 Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome Miyake, Noriko
2003
72 5 p. 1331-1337
7 p.
artikel
32 Reply to Silva et al. Yao, Yong-Gang
2003
72 5 p. 1348-1349
2 p.
artikel
33 Richard H. Ward, Ph.D. (June 7, 1943–February 14, 2003): Wild Ride of the Valkyries Weiss, Kenneth M.
2003
72 5 p. 1079-1083
5 p.
artikel
34 The CHEK2 1100delC Mutation Identifies Families with a Hereditary Breast and Colorectal Cancer Phenotype Meijers-Heijboer, Hanne
2003
72 5 p. 1308-1314
7 p.
artikel
35 The Emperor’s New Methods Spence, M. Anne
2003
72 5 p. 1084-1087
4 p.
artikel
36 This Month in the Journal Garber, Kathryn
2003
72 5 p. i-ii
nvt p.
artikel
37 To Trust or Not to Trust an Idiosyncratic Mitochondrial Data Set Yao, Yong-Gang
2003
72 5 p. 1341-1346
6 p.
artikel
                             37 gevonden resultaten
 
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