| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Common Haplotype of the Glucokinase Gene Alters Fasting Glucose and Birth Weight: Association in Six Studies and Population-Genetics Analyses
|
Weedon, Michael N.
|
|
|
79 |
6 |
p. 991-1001
|
artikel
|
| 2 |
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@ajhg.net. 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.
|
|
|
|
79 |
6 |
p. 1144-1146
|
artikel
|
| 3 |
ASHG Code of Ethics
|
Boughman, Joann A.
|
|
|
79 |
6 |
p. 1136-1137
|
artikel
|
| 4 |
Biochemical and Genetic Analysis of ANK in Arthritis and Bone Disease
|
Gurley, Kyle A.
|
|
|
79 |
6 |
p. 1017-1029
|
artikel
|
| 5 |
Contents of Volume 79
|
|
|
|
79 |
6 |
p. 1147-1160
|
artikel
|
| 6 |
Editorial Reviewers for 2006
|
|
|
|
79 |
6 |
p. 1138-1143
|
artikel
|
| 7 |
Erratum
|
|
|
|
79 |
6 |
p. 1135
|
artikel
|
| 8 |
Exact Tests of Hardy-Weinberg Equilibrium and Homogeneity of Disequilibrium across Strata
|
Schaid, Daniel J.
|
|
|
79 |
6 |
p. 1071-1080
|
artikel
|
| 9 |
Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci
|
Bisceglia, Luigi
|
|
|
79 |
6 |
p. 1130-1134
|
artikel
|
| 10 |
HLA and Genomewide Allele Sharing in Dizygotic Twins
|
Montgomery, Grant W.
|
|
|
79 |
6 |
p. 1052-1058
|
artikel
|
| 11 |
Human Adaptive Evolution at Myostatin (GDF8), a Regulator of Muscle Growth
|
Saunders, Matthew A.
|
|
|
79 |
6 |
p. 1089-1097
|
artikel
|
| 12 |
Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III
|
Cichon, Sven
|
|
|
79 |
6 |
p. 1098-1104
|
artikel
|
| 13 |
Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations
|
López, Luis Carlos
|
|
|
79 |
6 |
p. 1125-1129
|
artikel
|
| 14 |
Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy
|
Heuser, Arnd
|
|
|
79 |
6 |
p. 1081-1088
|
artikel
|
| 15 |
Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation
|
Tarpey, Patrick S.
|
|
|
79 |
6 |
p. 1119-1124
|
artikel
|
| 16 |
Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia
|
Bergmann, C.
|
|
|
79 |
6 |
p. 1105-1109
|
artikel
|
| 17 |
Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure
|
Li, Duanxiang
|
|
|
79 |
6 |
p. 1030-1039
|
artikel
|
| 18 |
Powerful Multilocus Tests of Genetic Association in the Presence of Gene-Gene and Gene-Environment Interactions
|
Chatterjee, Nilanjan
|
|
|
79 |
6 |
p. 1002-1016
|
artikel
|
| 19 |
Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration
|
Friedman, James S.
|
|
|
79 |
6 |
p. 1059-1070
|
artikel
|
| 20 |
Ribosomal Protein S24 Gene Is Mutated in Diamond-Blackfan Anemia
|
Gazda, Hanna T.
|
|
|
79 |
6 |
p. 1110-1118
|
artikel
|
| 21 |
This Month in the Journal
|
Williamson, Robin E.
|
|
|
79 |
6 |
p. i-ii
|
artikel
|
| 22 |
Tricellulin Is a Tight-Junction Protein Necessary for Hearing
|
Riazuddin, Saima
|
|
|
79 |
6 |
p. 1040-1051
|
artikel
|
Tijdschrift beschrijving