| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Genomewide Scan for Age-Related Macular Degeneration Provides Evidence for Linkage to Several Chromosomal Regions
|
Seddon, Johanna M.
|
|
2003
|
73 |
4 |
p. 780-790
11 p.
|
artikel
|
| 2 |
A Genomewide Screen of 345 Families for Autism-Susceptibility Loci
|
Yonan, Amanda L.
|
|
2003
|
73 |
4 |
p. 886-897
12 p.
|
artikel
|
| 3 |
An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications
|
Bailey, Jeffrey A.
|
|
2003
|
73 |
4 |
p. 823-834
12 p.
|
artikel
|
| 4 |
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.
|
|
|
2003
|
73 |
4 |
p. 976-978
3 p.
|
artikel
|
| 5 |
“Are We There Yet?”: Deciding When One Has Demonstrated Specific Genetic Causation in Complex Diseases and Quantitative Traits
|
Page, Grier P.
|
|
2003
|
73 |
4 |
p. 711-719
9 p.
|
artikel
|
| 6 |
Common and Unique Susceptibility Loci in Graves and Hashimoto Diseases: Results of Whole-Genome Screening in a Data Set of 102 Multiplex Families
|
Tomer, Yaron
|
|
2003
|
73 |
4 |
p. 736-747
12 p.
|
artikel
|
| 7 |
Confirmation of the Type 2 Myotonic Dystrophy (CCTG) n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect
|
Bachinski, Linda L.
|
|
2003
|
73 |
4 |
p. 835-848
14 p.
|
artikel
|
| 8 |
Erratum
|
|
|
2003
|
73 |
4 |
p. 979-
1 p.
|
artikel
|
| 9 |
Erroneous Claims about the Impact of Mitochondrial DNA Sequence Database Errors
|
Helgason, Agnar
|
|
2003
|
73 |
4 |
p. 974-975
2 p.
|
artikel
|
| 10 |
Genomewide Linkage and Linkage Disequilibrium Analyses Identify COL6A1, on Chromosome 21, as the Locus for Ossification of the Posterior Longitudinal Ligament of the Spine
|
Tanaka, Toshihiro
|
|
2003
|
73 |
4 |
p. 812-822
11 p.
|
artikel
|
| 11 |
Genomic Imprinting and Linkage Test for Quantitative-Trait Loci in Extended Pedigrees
|
Shete, Sanjay
|
|
2003
|
73 |
4 |
p. 933-938
6 p.
|
artikel
|
| 12 |
HLA-DRB1*1101: A Significant Risk Factor for Sarcoidosis in Blacks and Whites
|
Rossman, Milton D.
|
|
2003
|
73 |
4 |
p. 720-735
16 p.
|
artikel
|
| 13 |
Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons
|
Chai, J-H.
|
|
2003
|
73 |
4 |
p. 898-925
28 p.
|
artikel
|
| 14 |
Loss of CpG Methylation Is Strongly Correlated with Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients with Beckwith-Wiedemann Syndrome
|
Higashimoto, Ken
|
|
2003
|
73 |
4 |
p. 948-956
9 p.
|
artikel
|
| 15 |
Multiple Origins of Ashkenazi Levites: Y Chromosome Evidence for Both Near Eastern and European Ancestries
|
Behar, Doron M.
|
|
2003
|
73 |
4 |
p. 768-779
12 p.
|
artikel
|
| 16 |
Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
|
Dowling, Oonagh
|
|
2003
|
73 |
4 |
p. 957-966
10 p.
|
artikel
|
| 17 |
Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
|
Hanks, Sandra
|
|
2003
|
73 |
4 |
p. 791-800
10 p.
|
artikel
|
| 18 |
Myotonic Dystrophy Type 2: Human Founder Haplotype and Evolutionary Conservation of the Repeat Tract
|
Liquori, Christina L.
|
|
2003
|
73 |
4 |
p. 849-862
14 p.
|
artikel
|
| 19 |
NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)
|
Rainier, Shirley
|
|
2003
|
73 |
4 |
p. 967-971
5 p.
|
artikel
|
| 20 |
Pooled Analysis of Loss of Heterozygosity in Breast Cancer: a Genome Scan Provides Comparative Evidence for Multiple Tumor Suppressors and Identifies Novel Candidate Regions
|
Miller, Brian J.
|
|
2003
|
73 |
4 |
p. 748-767
20 p.
|
artikel
|
| 21 |
Recent Advances in Human Quantitative-Trait–Locus Mapping: Comparison of Methods for Discordant Sibling Pairs
|
Szatkiewicz, Jin P.
|
|
2003
|
73 |
4 |
p. 874-885
12 p.
|
artikel
|
| 22 |
Recent Advances in Human Quantitative-Trait–Locus Mapping: Comparison of Methods for Selected Sibling Pairs
|
T.Cuenco, Karen
|
|
2003
|
73 |
4 |
p. 863-873
11 p.
|
artikel
|
| 23 |
SCA8 Repeat Expansion Coexists with SCA1—Not Only with SCA6
|
Sulek, Anna
|
|
2003
|
73 |
4 |
p. 972-974
3 p.
|
artikel
|
| 24 |
Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10
|
Verhoeven, Kristien
|
|
2003
|
73 |
4 |
p. 926-932
7 p.
|
artikel
|
| 25 |
The Paternal-Age Effect in Apert Syndrome Is Due, in Part, to the Increased Frequency of Mutations in Sperm
|
Glaser, Rivka L.
|
|
2003
|
73 |
4 |
p. 939-947
9 p.
|
artikel
|
| 26 |
This Month in the Journal
|
Garber, Kathryn
|
|
2003
|
73 |
4 |
p. i-ii
nvt p.
|
artikel
|
| 27 |
Using the Noninformative Families in Family-Based Association Tests: A Powerful New Testing Strategy
|
Lange, Christoph
|
|
2003
|
73 |
4 |
p. 801-811
11 p.
|
artikel
|
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