| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Affected-Sib-Pair Data Can Be Used to Distinguish Two-Locus Heterogeneity from Two-Locus Epistasis
|
Cordell, Heather J.
|
|
2003
|
73 |
6 |
p. 1468-1470
3 p.
|
artikel
|
| 2 |
Allelic Heterogeneity in LINE-1 Retrotransposition Activity
|
Lutz, Sheila M.
|
|
2003
|
73 |
6 |
p. 1431-1437
7 p.
|
artikel
|
| 3 |
Announcements 1 1 Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please mail announcements to The American Journal of Human Genetics, Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Room 301, Atlanta, GA 30322-3050; fax them to (404) 712-9984; or send via E-mail to ajhg@emory.edu. Submission must be received at least 7 weeks before the month of issue in which publication is requested. They must be double spaced with a 1½-inch margin on all sides. The maximum length is 250 words, excluding the address for correspondence. Please include a cover letter indicating the name of the sponsoring ASHG member.
|
|
|
2003
|
73 |
6 |
p. 1474-1476
3 p.
|
artikel
|
| 4 |
A Novel Claudin 16 Mutation Associated with Childhood Hypercalciuria Abolishes Binding to ZO-1 and Results in Lysosomal Mistargeting
|
Müller, Dominik
|
|
2003
|
73 |
6 |
p. 1293-1301
9 p.
|
artikel
|
| 5 |
Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities
|
Vissers, Lisenka E.L.M.
|
|
2003
|
73 |
6 |
p. 1261-1270
10 p.
|
artikel
|
| 6 |
A Systematic Genomewide Linkage Study in 353 Sib Pairs with Schizophrenia
|
Williams, N.M.
|
|
2003
|
73 |
6 |
p. 1355-1367
13 p.
|
artikel
|
| 7 |
Capillary Malformation–Arteriovenous Malformation, a New Clinical and Genetic Disorder Caused by RASA1 Mutations
|
Eerola, Iiro
|
|
2003
|
73 |
6 |
p. 1240-1249
10 p.
|
artikel
|
| 8 |
Cockayne Syndrome Group B Cellular and Biochemical Functions
|
Licht, Cecilie Löe
|
|
2003
|
73 |
6 |
p. 1217-1239
23 p.
|
artikel
|
| 9 |
Comparative Linkage-Disequilibrium Analysis of the β-Globin Hotspot in Primates
|
Wall, Jeffrey D.
|
|
2003
|
73 |
6 |
p. 1330-1340
11 p.
|
artikel
|
| 10 |
Dominant Intermediate Charcot-Marie-Tooth Type C Maps to Chromosome 1p34-p35
|
Jordanova, Albena
|
|
2003
|
73 |
6 |
p. 1423-1430
8 p.
|
artikel
|
| 11 |
Editorial Reviewers for 2003
|
|
|
2003
|
73 |
6 |
p. i-vi
nvt p.
|
artikel
|
| 12 |
Erratum
|
|
|
2003
|
73 |
6 |
p. 1477-
1 p.
|
artikel
|
| 13 |
Erratum
|
|
|
2003
|
73 |
6 |
p. 1470-
1 p.
|
artikel
|
| 14 |
Fine-Scale Mapping of Disease Genes with Multiple Mutations via Spatial Clustering Techniques
|
Molitor, John
|
|
2003
|
73 |
6 |
p. 1368-1384
17 p.
|
artikel
|
| 15 |
Further Evidence of IBD5/CARD15 (NOD2) Epistasis in the Susceptibility to Ulcerative Colitis
|
McGovern, Dermot P.B.
|
|
2003
|
73 |
6 |
p. 1465-1466
2 p.
|
artikel
|
| 16 |
Genetic Anthropology of the Colorectal Cancer–Susceptibility Allele APC I1307K: Evidence of Genetic Drift within the Ashkenazim
|
Niell, Bethany L.
|
|
2003
|
73 |
6 |
p. 1250-1260
11 p.
|
artikel
|
| 17 |
Inference on Haplotype Effects in Case-Control Studies Using Unphased Genotype Data
|
Epstein, Michael P.
|
|
2003
|
73 |
6 |
p. 1316-1329
14 p.
|
artikel
|
| 18 |
Informativeness of Genetic Markers for Inference of Ancestry*
|
Rosenberg, Noah A.
|
|
2003
|
73 |
6 |
p. 1402-1422
21 p.
|
artikel
|
| 19 |
MDR1 Ala893 Polymorphism Is Associated with Inflammatory Bowel Disease
|
Brant, Steven R.
|
|
2003
|
73 |
6 |
p. 1282-1292
11 p.
|
artikel
|
| 20 |
Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations
|
Liquori, Christina L.
|
|
2003
|
73 |
6 |
p. 1459-1464
6 p.
|
artikel
|
| 21 |
Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation
|
Shoichet, Sarah A.
|
|
2003
|
73 |
6 |
p. 1341-1354
14 p.
|
artikel
|
| 22 |
Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2
|
Abkevich, Victor
|
|
2003
|
73 |
6 |
p. 1271-1281
11 p.
|
artikel
|
| 23 |
Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study
|
del Castillo, Ignacio
|
|
2003
|
73 |
6 |
p. 1452-1458
7 p.
|
artikel
|
| 24 |
Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2
|
Bi, Weimin
|
|
2003
|
73 |
6 |
p. 1302-1315
14 p.
|
artikel
|
| 25 |
Reply to Cordell and Farrall
|
Vieland, Veronica J.
|
|
2003
|
73 |
6 |
p. 1471-1473
3 p.
|
artikel
|
| 26 |
Reports of the Death of the Epistasis Model Are Greatly Exaggerated
|
Farrall, Martin
|
|
2003
|
73 |
6 |
p. 1467-1468
2 p.
|
artikel
|
| 27 |
Search for Haplotype Interactions That Influence Susceptibility to Type 1 Diabetes, through Use of Unphased Genotype Data
|
Zhang, Jian
|
|
2003
|
73 |
6 |
p. 1385-1401
17 p.
|
artikel
|
| 28 |
SVA Elements Are Nonautonomous Retrotransposons that Cause Disease in Humans
|
Ostertag, Eric M.
|
|
2003
|
73 |
6 |
p. 1444-1451
8 p.
|
artikel
|
| 29 |
The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease
|
Van Den Bogaert, Ann
|
|
2003
|
73 |
6 |
p. 1438-1443
6 p.
|
artikel
|
| 30 |
This Month in the Journal
|
Garber, Kathryn
|
|
2003
|
73 |
6 |
p. vii-viii
nvt p.
|
artikel
|
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