nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Constrained-Likelihood Approach to Marker-Trait Association Studies
|
Wang, Kai |
|
2005 |
77 |
5 |
p. 768-780 13 p. |
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.
|
|
|
2005 |
77 |
5 |
p. 899-901 3 p. |
artikel |
3 |
A Novel Method with Improved Power To Detect Recombination Hotspots from Polymorphism Data Reveals Multiple Hotspots in Human Genes
|
Fearnhead, Paul |
|
2005 |
77 |
5 |
p. 781-794 14 p. |
artikel |
4 |
Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor
|
Niemitz, Emily L. |
|
2005 |
77 |
5 |
p. 887-891 5 p. |
artikel |
5 |
Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome
|
Ai, Minrong |
|
2005 |
77 |
5 |
p. 741-753 13 p. |
artikel |
6 |
Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants
|
Khajavi, Mehrdad |
|
2005 |
77 |
5 |
p. 841-850 10 p. |
artikel |
7 |
Erratum
|
|
|
2005 |
77 |
5 |
p. 898- 1 p. |
artikel |
8 |
Evidence for Widespread Reticulate Evolution within Human Duplicons
|
Jackson, Michael S. |
|
2005 |
77 |
5 |
p. 824-840 17 p. |
artikel |
9 |
Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment.
|
Bennett, Robin L. |
|
2005 |
77 |
5 |
p. 896- 1 p. |
artikel |
10 |
Genetics of Developmental Disabilities.
|
Vekemans, Michel |
|
2005 |
77 |
5 |
p. 896-897 2 p. |
artikel |
11 |
Handling Marker-Marker Linkage Disequilibrium: Pedigree Analysis with Clustered Markers
|
Abecasis, Gonçalo R. |
|
2005 |
77 |
5 |
p. 754-767 14 p. |
artikel |
12 |
High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs
|
Slater, Howard R. |
|
2005 |
77 |
5 |
p. 709-726 18 p. |
artikel |
13 |
High-Resolution Whole-Genome Association Study of Parkinson Disease
|
Maraganore, Demetrius M. |
|
2005 |
77 |
5 |
p. 685-693 9 p. |
artikel |
14 |
Multiple Correcting COL17A1 Mutations in Patients with Revertant Mosaicism of Epidermolysis Bullosa
|
Pasmooij, Anna M.G. |
|
2005 |
77 |
5 |
p. 727-740 14 p. |
artikel |
15 |
Mutations in TCF8 Cause Posterior Polymorphous Corneal Dystrophy and Ectopic Expression of COL4A3 by Corneal Endothelial Cells
|
Krafchak, Charles M. |
|
2005 |
77 |
5 |
p. 694-708 15 p. |
artikel |
16 |
Narrowing the Candidate Region for Congenital Diaphragmatic Hernia in Chromosome 15q26: Contradictory Results
|
Castiglia, L. |
|
2005 |
77 |
5 |
p. 892-894 3 p. |
artikel |
17 |
Promoter and 3′-Untranslated-Region Haplotypes in the Vitamin D Receptor Gene Predispose to Osteoporotic Fracture: The Rotterdam Study
|
Fang, Yue |
|
2005 |
77 |
5 |
p. 807-823 17 p. |
artikel |
18 |
Reply to Castiglia et al.
|
Klaassens, M. |
|
2005 |
77 |
5 |
p. 894-895 2 p. |
artikel |
19 |
Severely Incapacitating Mutations in Patients with Extreme Short Stature Identify RNA-Processing Endoribonuclease RMRP as an Essential Cell Growth Regulator
|
Thiel, Christian T. |
|
2005 |
77 |
5 |
p. 795-806 12 p. |
artikel |
20 |
Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus
|
Benayed, Rym |
|
2005 |
77 |
5 |
p. 851-868 18 p. |
artikel |
21 |
The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L Region
|
Barreiro, Luis B. |
|
2005 |
77 |
5 |
p. 869-886 18 p. |
artikel |
22 |
This Month in the Journal
|
Garber, Kathryn |
|
2005 |
77 |
5 |
p. i-ii nvt p. |
artikel |