| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Genomewide Linkage Screen for Relative Hand Skill in Sibling Pairs
|
Francks, Clyde
|
|
2002
|
70 |
3 |
p. 800-805
6 p.
|
artikel
|
| 2 |
A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13
|
Meijer, I.A.
|
|
2002
|
70 |
3 |
p. 763-769
7 p.
|
artikel
|
| 3 |
Announcements 1 1. Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please mail announcements to The American Journal of Human Genetics, Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Room 301, Atlanta, GA 30322-3050; fax them to (404) 712-9984; or send via E-mail 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.
|
|
|
2002
|
70 |
3 |
p. 822-828
7 p.
|
artikel
|
| 4 |
A Polymorphism in the Agouti Signaling Protein Gene Is Associated with Human Pigmentation
|
Kanetsky, Peter A.
|
|
2002
|
70 |
3 |
p. 770-775
6 p.
|
artikel
|
| 5 |
A Polymorphism in the Human UGRP1 Gene Promoter That Regulates Transcription Is Associated with an Increased Risk of Asthma
|
Niimi, Tomoaki
|
|
2002
|
70 |
3 |
p. 718-725
8 p.
|
artikel
|
| 6 |
A Quantitative-Trait Locus in the Human Factor XII Gene Influences Both Plasma Factor XII Levels and Susceptibility to Thrombotic Disease
|
Soria, José Manuel
|
|
2002
|
70 |
3 |
p. 567-574
8 p.
|
artikel
|
| 7 |
Association between Single-Nucleotide Polymorphisms in Selectin Genes and Immunoglobulin A Nephropathy
|
Takei, Takashi
|
|
2002
|
70 |
3 |
p. 781-786
6 p.
|
artikel
|
| 8 |
Association of Polymorphisms in the Apolipoprotein E Region with Susceptibility to and Progression of Multiple Sclerosis
|
Schmidt, Silke
|
|
2002
|
70 |
3 |
p. 708-717
10 p.
|
artikel
|
| 9 |
A Susceptibility Locus for Migraine with Aura, on Chromosome 4q24
|
Wessman, Maija
|
|
2002
|
70 |
3 |
p. 652-662
11 p.
|
artikel
|
| 10 |
A Variation in 3′ UTR of hPTP1B Increases Specific Gene Expression and Associates with Insulin Resistance
|
Di Paola, Rosa
|
|
2002
|
70 |
3 |
p. 806-812
7 p.
|
artikel
|
| 11 |
Bias in Estimates of Quantitative-Trait–Locus Effect in Genome Scans: Demonstration of the Phenomenon and a Method-of-Moments Procedure for Reducing Bias
|
Allison, David B.
|
|
2002
|
70 |
3 |
p. 575-585
11 p.
|
artikel
|
| 12 |
CFC1 Mutations in Patients with Transposition of the Great Arteries and Double-Outlet Right Ventricle
|
Goldmuntz, Elizabeth
|
|
2002
|
70 |
3 |
p. 776-780
5 p.
|
artikel
|
| 13 |
Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects
|
DeBaun, Michael R.
|
|
2002
|
70 |
3 |
p. 604-611
8 p.
|
artikel
|
| 14 |
Ethnic-Difference Markers for Use in Mapping by Admixture Linkage Disequilibrium
|
Collins-Schramm, Heather E.
|
|
2002
|
70 |
3 |
p. 737-750
14 p.
|
artikel
|
| 15 |
Evidence for a Susceptibility Gene for Anorexia Nervosa on Chromosome 1
|
Grice, D.E.
|
|
2002
|
70 |
3 |
p. 787-792
6 p.
|
artikel
|
| 16 |
Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin
|
Garner, Chad P.
|
|
2002
|
70 |
3 |
p. 793-799
7 p.
|
artikel
|
| 17 |
Extensive Linkage Disequilibrium in Small Human Populations in Eurasia
|
Kaessmann, Henrik
|
|
2002
|
70 |
3 |
p. 673-685
13 p.
|
artikel
|
| 18 |
Fine-Scale Mapping of Disease Loci via Shattered Coalescent Modeling of Genealogies
|
Morris, A.P.
|
|
2002
|
70 |
3 |
p. 686-707
22 p.
|
artikel
|
| 19 |
Glutamine Repeats and Neurodegenerative Diseases: Molecular Aspects
|
La Spada, Albert R.
|
|
2002
|
70 |
3 |
p. 820-821
2 p.
|
artikel
|
| 20 |
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
|
De Sandre-Giovannoli, Annachiara
|
|
2002
|
70 |
3 |
p. 726-736
11 p.
|
artikel
|
| 21 |
Individual-Specific Liability Groups in Genetic Linkage, with Applications to Kindreds with Li-Fraumeni Syndrome
|
Shete, Sanjay
|
|
2002
|
70 |
3 |
p. 813-817
5 p.
|
artikel
|
| 22 |
Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene
|
Frosk, Patrick
|
|
2002
|
70 |
3 |
p. 663-672
10 p.
|
artikel
|
| 23 |
Localization of a Gene for Peripheral Arterial Occlusive Disease to Chromosome 1p31
|
Gudmundsson, Gudmundur
|
|
2002
|
70 |
3 |
p. 586-592
7 p.
|
artikel
|
| 24 |
Localization of a Susceptibility Gene for Common Forms of Stroke to 5q12
|
Gretarsdottir, Solveig
|
|
2002
|
70 |
3 |
p. 593-603
11 p.
|
artikel
|
| 25 |
Mutational Spectrum in the PEX7 Gene and Functional Analysis of Mutant Alleles in 78 Patients with Rhizomelic Chondrodysplasia Punctata Type 1
|
Motley, Alison M.
|
|
2002
|
70 |
3 |
p. 612-624
13 p.
|
artikel
|
| 26 |
Mutation Patterns at Dinucleotide Microsatellite Loci in Humans
|
Huang, Qing-Yang
|
|
2002
|
70 |
3 |
p. 625-634
10 p.
|
artikel
|
| 27 |
Phylogeographic Differentiation of Mitochondrial DNA in Han Chinese
|
Yao, Yong-Gang
|
|
2002
|
70 |
3 |
p. 635-651
17 p.
|
artikel
|
| 28 |
Sibling Recurrence Risk Ratio as a Measure of Genetic Effect: Caveat Emptor!
|
Guo, Sun-Wei
|
|
2002
|
70 |
3 |
p. 818-819
2 p.
|
artikel
|
| 29 |
Testing for Genetic Linkage in Families by a Variance-Components Approach in the Presence of Genomic Imprinting
|
Shete, Sanjay
|
|
2002
|
70 |
3 |
p. 751-757
7 p.
|
artikel
|
| 30 |
The Frequent 5,10-Methylenetetrahydrofolate Reductase C677T Polymorphism Is Associated with a Common Haplotype in Whites, Japanese, and Africans
|
Rosenberg, Nurit
|
|
2002
|
70 |
3 |
p. 758-762
5 p.
|
artikel
|
| 31 |
This Month in the Journal
|
Beauregard, Kathryn
|
|
2002
|
70 |
3 |
p. i-ii
nvt p.
|
artikel
|
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