| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Age-Related Maculopathy: A Genomewide Scan with Continued Evidence of Susceptibility Loci within the 1q31, 10q26, and 17q25 Regions
|
Weeks, Daniel E.
|
|
2004
|
75 |
2 |
p. 174-189
16 p.
|
artikel
|
| 2 |
A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis
|
Begovich, Ann B.
|
|
2004
|
75 |
2 |
p. 330-337
8 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 ½-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.
|
|
|
2004
|
75 |
2 |
p. 351-
1 p.
|
artikel
|
| 4 |
A Population-Genetic Test of Founder Effects and Implications for Ashkenazi Jewish Diseases
|
Slatkin, Montgomery
|
|
2004
|
75 |
2 |
p. 282-293
12 p.
|
artikel
|
| 5 |
A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa
|
Arredi, Barbara
|
|
2004
|
75 |
2 |
p. 338-345
8 p.
|
artikel
|
| 6 |
A Susceptibility Locus for Myopia in the Normal Population Is Linked to the PAX6 Gene Region on Chromosome 11: A Genomewide Scan of Dizygotic Twins
|
Hammond, Christopher J.
|
|
2004
|
75 |
2 |
p. 294-304
11 p.
|
artikel
|
| 7 |
Authenticity of Ancient-DNA Results: A Statistical Approach
|
Spencer, Matthew
|
|
2004
|
75 |
2 |
p. 240-250
11 p.
|
artikel
|
| 8 |
Autosomal Dominant Avascular Necrosis of Femoral Head in Two Taiwanese Pedigrees and Linkage to Chromosome 12q13
|
Chen, Wei-Ming
|
|
2004
|
75 |
2 |
p. 310-317
8 p.
|
artikel
|
| 9 |
Common Variants in the 5′ Region of the Leptin Gene Are Associated with Body Mass Index in Men from the National Heart, Lung, and Blood Institute Family Heart Study
|
Jiang, Y.
|
|
2004
|
75 |
2 |
p. 220-230
11 p.
|
artikel
|
| 10 |
Erratum
|
|
|
2004
|
75 |
2 |
p. 352-
1 p.
|
artikel
|
| 11 |
Genomewide Linkage Scan for Bipolar-Disorder Susceptibility Loci among Ashkenazi Jewish Families
|
Fallin, M. Daniele
|
|
2004
|
75 |
2 |
p. 204-219
16 p.
|
artikel
|
| 12 |
Genotype-Phenotype Correlations for Nervous System Tumors in Neurofibromatosis 2: A Population-Based Study
|
Baser, Michael E.
|
|
2004
|
75 |
2 |
p. 231-239
9 p.
|
artikel
|
| 13 |
High-Resolution Molecular Characterization of 15q11-q13 Rearrangements by Array Comparative Genomic Hybridization (Array CGH) with Detection of Gene Dosage
|
Wang, Nicholas J.
|
|
2004
|
75 |
2 |
p. 267-281
15 p.
|
artikel
|
| 14 |
Intergenerational Instability of the Expanded CTG Repeat in the DMPK Gene: Studies in Human Gametes and Preimplantation Embryos
|
Temmerman, Nele De
|
|
2004
|
75 |
2 |
p. 325-329
5 p.
|
artikel
|
| 15 |
Jane M. Olson (December 6, 1952–May 2, 2004)
|
Elston, Robert C.
|
|
2004
|
75 |
2 |
p. 159-160
2 p.
|
artikel
|
| 16 |
Large-Scale Single-Nucleotide Polymorphism (SNP) and Haplotype Analyses, Using Dense SNP Maps, of 199 Drug-Related Genes in 752 Subjects: the Analysis of the Association between Uncommon SNPs within Haplotype Blocks and the Haplotypes Constructed with Haplotype-Tagging SNPs
|
Kamatani, Naoyuki
|
|
2004
|
75 |
2 |
p. 190-203
14 p.
|
artikel
|
| 17 |
Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35
|
Marazita, Mary L.
|
|
2004
|
75 |
2 |
p. 161-173
13 p.
|
artikel
|
| 18 |
Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation
|
Trimborn, Marc
|
|
2004
|
75 |
2 |
p. 261-266
6 p.
|
artikel
|
| 19 |
Mutations in the DLG3 Gene Cause Nonsyndromic X-Linked Mental Retardation
|
Tarpey, Patrick
|
|
2004
|
75 |
2 |
p. 318-324
7 p.
|
artikel
|
| 20 |
Mutations in the FTSJ1 Gene Coding for a Novel S-Adenosylmethionine–Binding Protein Cause Nonsyndromic X-Linked Mental Retardation
|
Freude, Kristine
|
|
2004
|
75 |
2 |
p. 305-309
5 p.
|
artikel
|
| 21 |
Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease
|
Uhlenberg, Birgit
|
|
2004
|
75 |
2 |
p. 251-260
10 p.
|
artikel
|
| 22 |
SLEN2 (2q34–35) and SLEN1 (10q22.3) Replication in Systemic Lupus Erythematosus Stratified by Nephritis
|
Quintero-Del-Rio, Ana I.
|
|
2004
|
75 |
2 |
p. 346-348
3 p.
|
artikel
|
| 23 |
The Hereditary Basis of Allergic Disease
|
Kruse, Torben A.
|
|
2004
|
75 |
2 |
p. 349-350
2 p.
|
artikel
|
| 24 |
This Month in the Journal
|
Garber, Kathryn
|
|
2004
|
75 |
2 |
p. i-ii
nvt p.
|
artikel
|
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