| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
|
Schwartz, Charles E.
|
|
2005
|
77 |
1 |
p. 41-53
13 p.
|
artikel
|
| 2 |
An Entropy-Based Statistic for Genomewide Association Studies
|
Zhao, Jinying
|
|
2005
|
77 |
1 |
p. 27-40
14 p.
|
artikel
|
| 3 |
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@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.
|
|
|
2005
|
77 |
1 |
p. 169-
1 p.
|
artikel
|
| 4 |
A Powerful and Robust Method for Mapping Quantitative Trait Loci in General Pedigrees
|
Diao, G.
|
|
2005
|
77 |
1 |
p. 97-111
15 p.
|
artikel
|
| 5 |
Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3
|
Zeng, Wen-Qi
|
|
2005
|
77 |
1 |
p. 16-26
11 p.
|
artikel
|
| 6 |
Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS
|
Mendoza-Londono, Roberto
|
|
2005
|
77 |
1 |
p. 161-168
8 p.
|
artikel
|
| 7 |
Disentangling Fetal and Maternal Susceptibility for Pre-Eclampsia: A British Multicenter Candidate-Gene Study
|
|
|
2005
|
77 |
1 |
p. 127-131
5 p.
|
artikel
|
| 8 |
Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
|
Hillmer, Axel M.
|
|
2005
|
77 |
1 |
p. 140-148
9 p.
|
artikel
|
| 9 |
Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects
|
Farrington, Susan M.
|
|
2005
|
77 |
1 |
p. 112-119
8 p.
|
artikel
|
| 10 |
Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems
|
Brooks, Alice S.
|
|
2005
|
77 |
1 |
p. 120-126
7 p.
|
artikel
|
| 11 |
Identification of a Major Recombination Hotspot in Patients with Short Stature and SHOX Deficiency
|
Schneider, Katja U.
|
|
2005
|
77 |
1 |
p. 89-96
8 p.
|
artikel
|
| 12 |
Identifying Novel Genes for Atherosclerosis through Mouse-Human Comparative Genetics
|
Wang, Xiaosong
|
|
2005
|
77 |
1 |
p. 1-15
15 p.
|
artikel
|
| 13 |
Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells
|
McDaniel, Lisa D.
|
|
2005
|
77 |
1 |
p. 132-139
8 p.
|
artikel
|
| 14 |
Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy
|
Li, Shouling
|
|
2005
|
77 |
1 |
p. 54-63
10 p.
|
artikel
|
| 15 |
Polymorphisms within the C-Reactive Protein (CRP) Promoter Region Are Associated with Plasma CRP Levels
|
Carlson, Christopher S.
|
|
2005
|
77 |
1 |
p. 64-77
14 p.
|
artikel
|
| 16 |
3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome
|
Willatt, Lionel
|
|
2005
|
77 |
1 |
p. 154-160
7 p.
|
artikel
|
| 17 |
Segmental Duplications and Copy-Number Variation in the Human Genome
|
Sharp, Andrew J.
|
|
2005
|
77 |
1 |
p. 78-88
11 p.
|
artikel
|
| 18 |
Strong Association of the Y402H Variant in Complement Factor H at 1q32 with Susceptibility to Age-Related Macular Degeneration
|
Zareparsi, Sepideh
|
|
2005
|
77 |
1 |
p. 149-153
5 p.
|
artikel
|
| 19 |
This Month in the Journal
|
Garber, Kathryn
|
|
2005
|
77 |
1 |
p. i-ii
nvt p.
|
artikel
|
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