nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
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.
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2004 |
74 |
2 |
p. 370-371 2 p. |
artikel |
2 |
Are Variants in the CAPN10 Gene Related to Risk of Type 2 Diabetes? A Quantitative Assessment of Population and Family-Based Association Studies
|
Song, Yiqing |
|
2004 |
74 |
2 |
p. 208-222 15 p. |
artikel |
3 |
Both Rare and Common Polymorphisms Contribute Functional Variation at CHGA, a Regulator of Catecholamine Physiology
|
Wen, Gen |
|
2004 |
74 |
2 |
p. 197-207 11 p. |
artikel |
4 |
Comparative Genomics and the Evolution of Human Mitochondrial DNA: Assessing the Effects of Selection
|
Elson, J.L. |
|
2004 |
74 |
2 |
p. 229-238 10 p. |
artikel |
5 |
Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women
|
Econs, Michael J. |
|
2004 |
74 |
2 |
p. 223-228 6 p. |
artikel |
6 |
Erratum
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2004 |
74 |
2 |
p. 372- 1 p. |
artikel |
7 |
Ethylmalonic Encephalopathy Is Caused by Mutations in ETHE1, a Gene Encoding a Mitochondrial Matrix Protein
|
Tiranti, Valeria |
|
2004 |
74 |
2 |
p. 239-252 14 p. |
artikel |
8 |
Evidence of a Novel Quantitative-Trait Locus for Obesity on Chromosome 4p in Mexican Americans
|
Arya, Rector |
|
2004 |
74 |
2 |
p. 272-282 11 p. |
artikel |
9 |
Genomewide Linkage Analysis for Internal Carotid Artery Intimal Medial Thickness: Evidence for Linkage to Chromosome 12
|
Fox, Caroline S. |
|
2004 |
74 |
2 |
p. 253-261 9 p. |
artikel |
10 |
Inherent Bias toward the Null Hypothesis in Conventional Multipoint Nonparametric Linkage Analysis
|
Schork, Nicholas J. |
|
2004 |
74 |
2 |
p. 306-316 11 p. |
artikel |
11 |
Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes
|
Lowe, Naomi |
|
2004 |
74 |
2 |
p. 348-356 9 p. |
artikel |
12 |
Matching Strategies for Genetic Association Studies in Structured Populations
|
Hinds, David A. |
|
2004 |
74 |
2 |
p. 317-325 9 p. |
artikel |
13 |
Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II
|
Weston, Michael D. |
|
2004 |
74 |
2 |
p. 357-366 10 p. |
artikel |
14 |
Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations
|
Denier, C. |
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2004 |
74 |
2 |
p. 326-337 12 p. |
artikel |
15 |
Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome
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Dagoneau, Nathalie |
|
2004 |
74 |
2 |
p. 298-305 8 p. |
artikel |
16 |
Pathogenic Mutations Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Differently Affect Jagged1 Binding and Notch3 Activity via the RBP/JK Signaling Pathway
|
Joutel, Anne |
|
2004 |
74 |
2 |
p. 338-347 10 p. |
artikel |
17 |
PBAT: Tools for Family-Based Association Studies
|
Lange, Christoph |
|
2004 |
74 |
2 |
p. 367-369 3 p. |
artikel |
18 |
Pleiotropic Effects of a Chromosome 3 Locus on Speech-Sound Disorder and Reading
|
Stein, Catherine M. |
|
2004 |
74 |
2 |
p. 283-297 15 p. |
artikel |
19 |
Premature Myocardial Infarction Novel Susceptibility Locus on Chromosome 1P34-36 Identified by Genomewide Linkage Analysis
|
Wang, Qing |
|
2004 |
74 |
2 |
p. 262-271 10 p. |
artikel |
20 |
This Month in the Journal
|
Garber, Kathryn |
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2004 |
74 |
2 |
p. i-ii nvt p. |
artikel |