| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Genomewide Screen for Generalized Vitiligo: Confirmation of AIS1 on Chromosome 1p31 and Evidence for Additional Susceptibility Loci
|
Fain, Pamela R.
|
|
2003
|
72 |
6 |
p. 1560-1564
5 p.
|
artikel
|
| 2 |
A Locus for Autosomal Dominant Mitral Valve Prolapse on Chromosome 11p15.4
|
Freed, Lisa A.
|
|
2003
|
72 |
6 |
p. 1551-1559
9 p.
|
artikel
|
| 3 |
A Neutral Explanation for the Correlation of Diversity with Recombination Rates in Humans
|
Hellmann, Ines
|
|
2003
|
72 |
6 |
p. 1527-1535
9 p.
|
artikel
|
| 4 |
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.
|
|
|
2003
|
72 |
6 |
p. 1599-1601
3 p.
|
artikel
|
| 5 |
A Novel Class of Tests for the Detection of Mitochondrial DNA–Mutation Involvement in Diseases
|
Sun, Fengzhu
|
|
2003
|
72 |
6 |
p. 1515-1526
12 p.
|
artikel
|
| 6 |
A Populationwide Coalescent Analysis of Icelandic Matrilineal and Patrilineal Genealogies: Evidence for a Faster Evolutionary Rate of mtDNA Lineages than Y Chromosomes
|
Helgason, Agnar
|
|
2003
|
72 |
6 |
p. 1370-1388
19 p.
|
artikel
|
| 7 |
Association and Interaction of the IL4R, IL4, and IL13 Loci with Type 1 Diabetes among Filipinos
|
Bugawan, Teodorica L.
|
|
2003
|
72 |
6 |
p. 1505-1514
10 p.
|
artikel
|
| 8 |
Association of Specific Language Impairment (SLI) to the Region of 7q31
|
O’Brien, Erin K.
|
|
2003
|
72 |
6 |
p. 1536-1543
8 p.
|
artikel
|
| 9 |
A Whole-Genome Screen of a Quantitative Trait of Age-Related Maculopathy in Sibships from the Beaver Dam Eye Study
|
Schick, James H.
|
|
2003
|
72 |
6 |
p. 1412-1424
13 p.
|
artikel
|
| 10 |
Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport
|
Kolehmainen, Juha
|
|
2003
|
72 |
6 |
p. 1359-1369
11 p.
|
artikel
|
| 11 |
Control of Confounding of Genetic Associations in Stratified Populations
|
Hoggart, Clive J.
|
|
2003
|
72 |
6 |
p. 1492-1504
13 p.
|
artikel
|
| 12 |
Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH
|
Veltman, Joris A.
|
|
2003
|
72 |
6 |
p. 1578-1584
7 p.
|
artikel
|
| 13 |
Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation
|
Kalscheuer, Vera M.
|
|
2003
|
72 |
6 |
p. 1401-1411
11 p.
|
artikel
|
| 14 |
Errors, Phantom and Otherwise, in Human mtDNA Sequences
|
Herrnstadt, Corinna
|
|
2003
|
72 |
6 |
p. 1585-1586
2 p.
|
artikel
|
| 15 |
Essentials of Medical Genomics
|
Mealiffe, Matthew E.
|
|
2003
|
72 |
6 |
p. 1597-1598
2 p.
|
artikel
|
| 16 |
Familial and Ovarian Cancer: Genetics, Screening and Management
|
Peters, June
|
|
2003
|
72 |
6 |
p. 1596-1597
2 p.
|
artikel
|
| 17 |
Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3
|
Stefánsson, Stefán Einar
|
|
2003
|
72 |
6 |
p. 1448-1459
12 p.
|
artikel
|
| 18 |
Identification of a Novel Gene and a Common Variant Associated with Uric Acid Nephrolithiasis in a Sardinian Genetic Isolate
|
Gianfrancesco, Fernando
|
|
2003
|
72 |
6 |
p. 1479-1491
13 p.
|
artikel
|
| 19 |
Multiple Mutations ofMYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss
|
Donaudy, Francesca
|
|
2003
|
72 |
6 |
p. 1571-1577
7 p.
|
artikel
|
| 20 |
Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia
|
Irrthum, Alexandre
|
|
2003
|
72 |
6 |
p. 1470-1478
9 p.
|
artikel
|
| 21 |
Mutations of the PAX6 Gene Detected in Patients with a Variety of Optic-Nerve Malformations
|
Azuma, Noriyuki
|
|
2003
|
72 |
6 |
p. 1565-1570
6 p.
|
artikel
|
| 22 |
Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations
|
Fogli, Anne
|
|
2003
|
72 |
6 |
p. 1544-1550
7 p.
|
artikel
|
| 23 |
Reply to Bunce et al.
|
Copin, Bruno
|
|
2003
|
72 |
6 |
p. 1594-1595
2 p.
|
artikel
|
| 24 |
Reply to Cordaux and Stoneking
|
Endicott, Phillip
|
|
2003
|
72 |
6 |
p. 1590-1593
4 p.
|
artikel
|
| 25 |
Sequence Analysis of the Mitochondrial Genomes from Dutch Pedigrees with Leber Hereditary Optic Neuropathy
|
Howell, Neil
|
|
2003
|
72 |
6 |
p. 1460-1469
10 p.
|
artikel
|
| 26 |
Single-Nucleotide Polymorphisms and Glaucoma Severity
|
Bunce, Catey
|
|
2003
|
72 |
6 |
p. 1593-1594
2 p.
|
artikel
|
| 27 |
South Asia, the Andamanese, and the Genetic Evidence for an “Early” Human Dispersal out of Africa
|
Cordaux, Richard
|
|
2003
|
72 |
6 |
p. 1586-1590
5 p.
|
artikel
|
| 28 |
The Structure of Linkage Disequilibrium at the DBH Locus Strongly Influences the Magnitude of Association between Diallelic Markers and Plasma Dopamine β-Hydroxylase Activity
|
Zabetian, Cyrus P.
|
|
2003
|
72 |
6 |
p. 1389-1400
12 p.
|
artikel
|
| 29 |
This Month in the Journal
|
Garber, Kathryn
|
|
2003
|
72 |
6 |
p. i-ii
nvt p.
|
artikel
|
| 30 |
Two Modes of Germline Instability at Human Minisatellite MS1 (Locus D1S7): Complex Rearrangements and Paradoxical Hyperdeletion
|
Berg, Ingrid
|
|
2003
|
72 |
6 |
p. 1436-1447
12 p.
|
artikel
|
| 31 |
Variation in the HLA-G Promoter Region Influences Miscarriage Rates
|
Ober, Carole
|
|
2003
|
72 |
6 |
p. 1425-1435
11 p.
|
artikel
|
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