| 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@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.
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|
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2005
|
76 |
5 |
p. 908-910
3 p.
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artikel
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| 2 |
A Note on Exact Tests of Hardy-Weinberg Equilibrium
|
Wigginton, Janis E.
|
|
2005
|
76 |
5 |
p. 887-893
7 p.
|
artikel
|
| 3 |
A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS
|
Linglart, Agnès
|
|
2005
|
76 |
5 |
p. 804-814
11 p.
|
artikel
|
| 4 |
Autosomal Recessive Primary Microcephaly (MCPH): A Review of Clinical, Molecular, and Evolutionary Findings
|
Woods, C. Geoffrey
|
|
2005
|
76 |
5 |
p. 717-728
12 p.
|
artikel
|
| 5 |
Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization
|
Klaassens, M.
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2005
|
76 |
5 |
p. 877-882
6 p.
|
artikel
|
| 6 |
Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis
|
Huang, Ningwu
|
|
2005
|
76 |
5 |
p. 729-749
21 p.
|
artikel
|
| 7 |
Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome
|
Dhami, Pawandeep
|
|
2005
|
76 |
5 |
p. 750-762
13 p.
|
artikel
|
| 8 |
Identifying Candidate Hirschsprung Disease–Associated RET Variants
|
Burzynski, Grzegorz M.
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|
2005
|
76 |
5 |
p. 850-858
9 p.
|
artikel
|
| 9 |
Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design
|
Vitart, Veronique
|
|
2005
|
76 |
5 |
p. 763-772
10 p.
|
artikel
|
| 10 |
Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms
|
Vella, Adrian
|
|
2005
|
76 |
5 |
p. 773-779
7 p.
|
artikel
|
| 11 |
Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome
|
Yobb, Twila M.
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2005
|
76 |
5 |
p. 865-876
12 p.
|
artikel
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| 12 |
Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis
|
David Kelsell, P.
|
|
2005
|
76 |
5 |
p. 794-803
10 p.
|
artikel
|
| 13 |
Nonparametric Tests of Association of Multiple Genes with Human Disease
|
Schaid, Daniel J.
|
|
2005
|
76 |
5 |
p. 780-793
14 p.
|
artikel
|
| 14 |
Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism
|
Woods, Kathryn S.
|
|
2005
|
76 |
5 |
p. 833-849
17 p.
|
artikel
|
| 15 |
Quantitative Founder-Effect Analysis of French Canadian Families Identifies Specific Loci Contributing to Metabolic Phenotypes of Hypertension
|
Hamet, P.
|
|
2005
|
76 |
5 |
p. 815-832
18 p.
|
artikel
|
| 16 |
Saami and Berbers—An Unexpected Mitochondrial DNA Link
|
Achilli, Alessandro
|
|
2005
|
76 |
5 |
p. 883-886
4 p.
|
artikel
|
| 17 |
Single- and Multilocus Allelic Variants within the GABAB Receptor Subunit 2 (GABAB2) Gene Are Significantly Associated with Nicotine Dependence
|
Beuten, Joke
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|
2005
|
76 |
5 |
p. 859-864
6 p.
|
artikel
|
| 18 |
The Dual Origin of the Malagasy in Island Southeast Asia and East Africa: Evidence from Maternal and Paternal Lineages
|
Hurles, Matthew E.
|
|
2005
|
76 |
5 |
p. 894-901
8 p.
|
artikel
|
| 19 |
The Epsin 4 Gene on Chromosome 5q, Which Encodes the Clathrin-Associated Protein Enthoprotin, Is Involved in the Genetic Susceptibility to Schizophrenia
|
Pimm, Jonathan
|
|
2005
|
76 |
5 |
p. 902-907
6 p.
|
artikel
|
| 20 |
This Month in the Journal
|
Garber, Kathryn
|
|
2005
|
76 |
5 |
p. i-ii
nvt p.
|
artikel
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