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                             20 gevonden resultaten
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. 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 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.
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 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
2004
74 2 p. i-ii
nvt p.
artikel
                             20 gevonden resultaten
 
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