| 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 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.
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2006
|
79 |
1 |
p. 189-191
3 p.
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artikel
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| 2 |
Bayesian Graphical Models for Genomewide Association Studies
|
Verzilli, Claudio J.
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|
2006
|
79 |
1 |
p. 100-112
13 p.
|
artikel
|
| 3 |
Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease
|
Saxena, Richa
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2006
|
79 |
1 |
p. 54-61
8 p.
|
artikel
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| 4 |
Disruption of POF1B Binding to Nonmuscle Actin Filaments Is Associated with Premature Ovarian Failure
|
Lacombe, Arnaud
|
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2006
|
79 |
1 |
p. 113-119
7 p.
|
artikel
|
| 5 |
Distinct Expression Profiles for PTEN Transcript and Its Splice Variants in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome
|
Sarquis, Marta S.
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2006
|
79 |
1 |
p. 23-30
8 p.
|
artikel
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| 6 |
Double Inactivation of NF1 in Tibial Pseudarthrosis
|
Stevenson, David A.
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2006
|
79 |
1 |
p. 143-148
6 p.
|
artikel
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| 7 |
DSG2 Mutations Contribute to Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
|
Awad, Mark M.
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2006
|
79 |
1 |
p. 136-142
7 p.
|
artikel
|
| 8 |
ELMOD2 Is a Candidate Gene for Familial Idiopathic Pulmonary Fibrosis
|
Hodgson, Ulla
|
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2006
|
79 |
1 |
p. 149-154
6 p.
|
artikel
|
| 9 |
Expression of GJB2 and GJB6 Is Reduced in a Novel DFNB1 Allele
|
Wilch, Ellen
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2006
|
79 |
1 |
p. 174-179
6 p.
|
artikel
|
| 10 |
Familial Osteoarthritis of the Hip Joint Associated with Acetabular Dysplasia Maps to Chromosome 13q
|
Mabuchi, Akihiko
|
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2006
|
79 |
1 |
p. 163-168
6 p.
|
artikel
|
| 11 |
Genetic Variation in the CCL18-CCL3-CCL4 Chemokine Gene Cluster Influences HIV Type 1 Transmission and AIDS Disease Progression
|
Modi, William S.
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2006
|
79 |
1 |
p. 120-128
9 p.
|
artikel
|
| 12 |
Germline Missense Mutations Affecting KRAS Isoform B Are Associated with a Severe Noonan Syndrome Phenotype
|
Carta, Claudio
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2006
|
79 |
1 |
p. 129-135
7 p.
|
artikel
|
| 13 |
High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening *
|
Spada, Marco
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2006
|
79 |
1 |
p. 31-40
10 p.
|
artikel
|
| 14 |
Human Genomic Deletions Mediated by Recombination between Alu Elements
|
Sen, Shurjo K.
|
|
2006
|
79 |
1 |
p. 41-53
13 p.
|
artikel
|
| 15 |
Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly
|
Oates, N.A.
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2006
|
79 |
1 |
p. 155-162
8 p.
|
artikel
|
| 16 |
Intra- and Interindividual Epigenetic Variation in Human Germ Cells
|
Flanagan, James M.
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|
2006
|
79 |
1 |
p. 67-84
18 p.
|
artikel
|
| 17 |
Mapping Tumor-Suppressor Genes with Multipoint Statistics from Copy-Number–Variation Data
|
Ionita, Iuliana
|
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2006
|
79 |
1 |
p. 13-22
10 p.
|
artikel
|
| 18 |
NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway
|
McDaniell, Ryan
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2006
|
79 |
1 |
p. 169-173
5 p.
|
artikel
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| 19 |
Reconstructing Genetic Ancestry Blocks in Admixed Individuals
|
Tang, Hua
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2006
|
79 |
1 |
p. 1-12
12 p.
|
artikel
|
| 20 |
Reply to Bertram et al.
|
Grupe, Andrew
|
|
2006
|
79 |
1 |
p. 183-184
2 p.
|
artikel
|
| 21 |
Reply to Chappell et al.
|
DeMeo, Dawn L.
|
|
2006
|
79 |
1 |
p. 186-187
2 p.
|
artikel
|
| 22 |
Single-Nucleotide Polymorphism rs498055 on Chromosome 10q24 Is Not Associated with Alzheimer Disease in Two Independent Family Samples
|
Bertram, Lars
|
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2006
|
79 |
1 |
p. 180-183
4 p.
|
artikel
|
| 23 |
The Advocates Training Partnership Program
|
Boughman, Joann A.
|
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2006
|
79 |
1 |
p. 188-
1 p.
|
artikel
|
| 24 |
The SERPINE2 Gene and Chronic Obstructive Pulmonary Disease
|
Chappell, Sally
|
|
2006
|
79 |
1 |
p. 184-186
3 p.
|
artikel
|
| 25 |
This Month in the Journal
|
Williamson, Robin E.
|
|
2006
|
79 |
1 |
p. i-ii
nvt p.
|
artikel
|
| 26 |
Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine
|
Anttila, V.
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2006
|
79 |
1 |
p. 85-99
15 p.
|
artikel
|
| 27 |
Using Genomic Inbreeding Coefficient Estimates for Homozygosity Mapping of Rare Recessive Traits: Application to Taybi-Linder Syndrome
|
Leutenegger, Anne-Louise
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2006
|
79 |
1 |
p. 62-66
5 p.
|
artikel
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