| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A High-Density Screen for Linkage in Multiple Sclerosis
|
|
|
2005
|
77 |
3 |
p. 454-467
14 p.
|
artikel
|
| 2 |
A High-Density SNP Genomewide Linkage Scan for Chronic Lymphocytic Leukemia–Susceptibility Loci
|
Sellick, Gabrielle S.
|
|
2005
|
77 |
3 |
p. 420-429
10 p.
|
artikel
|
| 3 |
A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis
|
Gleghorn, Lindsay
|
|
2005
|
77 |
3 |
p. 484-490
7 p.
|
artikel
|
| 4 |
An Algorithm to Construct Genetically Similar Subsets of Families with the Use of Self-Reported Ethnicity Information
|
Skol, Andrew D.
|
|
2005
|
77 |
3 |
p. 346-354
9 p.
|
artikel
|
| 5 |
Announcements 1 1. Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements 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.
|
|
|
2005
|
77 |
3 |
p. 516-517
2 p.
|
artikel
|
| 6 |
Differential X Reactivation in Human Placental Cells: Implications for Reversal of X Inactivation
|
Migeon, Barbara R.
|
|
2005
|
77 |
3 |
p. 355-364
10 p.
|
artikel
|
| 7 |
Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males
|
Van Esch, Hilde
|
|
2005
|
77 |
3 |
p. 442-453
12 p.
|
artikel
|
| 8 |
Genetic Evidence for a Distinct Subtype of Schizophrenia Characterized by Pervasive Cognitive Deficit
|
Hallmayer, Joachim F.
|
|
2005
|
77 |
3 |
p. 468-476
9 p.
|
artikel
|
| 9 |
Genomewide Linkage Study in 1,176 Affected Sister Pair Families Identifies a Significant Susceptibility Locus for Endometriosis on Chromosome 10q26
|
Treloar, Susan A.
|
|
2005
|
77 |
3 |
p. 365-376
12 p.
|
artikel
|
| 10 |
Genomewide Significant Linkage to Migrainous Headache on Chromosome 5q21
|
Nyholt, Dale R.
|
|
2005
|
77 |
3 |
p. 500-512
13 p.
|
artikel
|
| 11 |
Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification
|
Boycott, Kym M.
|
|
2005
|
77 |
3 |
p. 477-483
7 p.
|
artikel
|
| 12 |
Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism
|
Ma, D.Q.
|
|
2005
|
77 |
3 |
p. 377-388
12 p.
|
artikel
|
| 13 |
Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin
|
Hakonen, Anna H.
|
|
2005
|
77 |
3 |
p. 430-441
12 p.
|
artikel
|
| 14 |
On Rapid Simulation of P Values in Association Studies
|
Lin, D.Y.
|
|
2005
|
77 |
3 |
p. 513-514
2 p.
|
artikel
|
| 15 |
Recent Developments in Genomewide Association Scans: A Workshop Summary and Review
|
Thomas, Duncan C.
|
|
2005
|
77 |
3 |
p. 337-345
9 p.
|
artikel
|
| 16 |
Reply to Lin
|
Seaman, S.R.
|
|
2005
|
77 |
3 |
p. 514-515
2 p.
|
artikel
|
| 17 |
Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26
|
Jakobsdottir, Johanna
|
|
2005
|
77 |
3 |
p. 389-407
19 p.
|
artikel
|
| 18 |
The BTNL2 Gene and Sarcoidosis Susceptibility in African Americans and Whites
|
Rybicki, Benjamin A.
|
|
2005
|
77 |
3 |
p. 491-499
9 p.
|
artikel
|
| 19 |
This Month in the Journal
|
Garber, Kathryn
|
|
2005
|
77 |
3 |
p. i-ii
nvt p.
|
artikel
|
| 20 |
Y-Chromosome Evidence of Southern Origin of the East Asian–Specific Haplogroup O3-M122
|
Shi, Hong
|
|
2005
|
77 |
3 |
p. 408-419
12 p.
|
artikel
|
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