| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Back Migration from Asia to Sub-Saharan Africa Is Supported by High-Resolution Analysis of Human Y-Chromosome Haplotypes
|
Cruciani, Fulvio
|
|
2002
|
70 |
5 |
p. 1197-1214
18 p.
|
artikel
|
| 2 |
A Combined Analysis of Genomewide Linkage Scans for Body Mass Index, from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
|
Wu, Xiaodong
|
|
2002
|
70 |
5 |
p. 1247-1256
10 p.
|
artikel
|
| 3 |
A Genomewide Linkage Scan for Quantitative-Trait Loci for Obesity Phenotypes
|
Deng, Hong-Wen
|
|
2002
|
70 |
5 |
p. 1138-1151
14 p.
|
artikel
|
| 4 |
A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder
|
Fisher, Simon E.
|
|
2002
|
70 |
5 |
p. 1183-1196
14 p.
|
artikel
|
| 5 |
A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family
|
Pras, Eran
|
|
2002
|
70 |
5 |
p. 1363-1367
5 p.
|
artikel
|
| 6 |
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 toajhg@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 ½-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 |
5 |
p. 1384-1387
4 p.
|
artikel
|
| 7 |
Common Deletion of SMAD4 in Juvenile Polyposis Is a Mutational Hotspot
|
Howe, James R.
|
|
2002
|
70 |
5 |
p. 1357-1362
6 p.
|
artikel
|
| 8 |
Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a SOD-1 Mutation: Potential Impact of CNTF as a Candidate Modifier Gene
|
Giess, Ralf
|
|
2002
|
70 |
5 |
p. 1277-1286
10 p.
|
artikel
|
| 9 |
ERRATUM
|
|
|
2002
|
70 |
5 |
p. 1388-
1 p.
|
artikel
|
| 10 |
Evidence for Linkage and Association with Reading Disability, on 6p21.3-22
|
Kaplan, D.E.
|
|
2002
|
70 |
5 |
p. 1287-1298
12 p.
|
artikel
|
| 11 |
FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment
|
Newbury, D.F.
|
|
2002
|
70 |
5 |
p. 1318-1327
10 p.
|
artikel
|
| 12 |
Generalized T 2 Test for Genome Association Studies
|
Xiong, Momiao
|
|
2002
|
70 |
5 |
p. 1257-1268
12 p.
|
artikel
|
| 13 |
Genetic Dissection of the Human Leukocyte Antigen Region by Use of Haplotypes of Tasmanians with Multiple Sclerosis
|
Rubio, Justin P.
|
|
2002
|
70 |
5 |
p. 1125-1137
13 p.
|
artikel
|
| 14 |
Genome Scans Provide Evidence for Low-HDL-C Loci on Chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish Families
|
Soro, Aino
|
|
2002
|
70 |
5 |
p. 1333-1340
8 p.
|
artikel
|
| 15 |
Genomewide Linkage Analysis of Quantitative Spirometric Phenotypes in Severe Early-Onset Chronic Obstructive Pulmonary Disease
|
Silverman, Edwin K.
|
|
2002
|
70 |
5 |
p. 1229-1239
11 p.
|
artikel
|
| 16 |
Genomic Disorders on 22q11
|
McDermid, Heather E.
|
|
2002
|
70 |
5 |
p. 1077-1088
12 p.
|
artikel
|
| 17 |
Geographic and Haplotype Structure of Candidate Type 2 Diabetes-Susceptibility Variants at the Calpain-10 Locus
|
Fullerton, Stephanie M.
|
|
2002
|
70 |
5 |
p. 1096-1106
11 p.
|
artikel
|
| 18 |
Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer
|
Rökman, Annika
|
|
2002
|
70 |
5 |
p. 1299-1304
6 p.
|
artikel
|
| 19 |
Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
|
Hansen, Jens Jacob
|
|
2002
|
70 |
5 |
p. 1328-1332
5 p.
|
artikel
|
| 20 |
High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization
|
Veltman, Joris A.
|
|
2002
|
70 |
5 |
p. 1269-1276
8 p.
|
artikel
|
| 21 |
Increased Rate of Twins among Affected Sibling Pairs with Autism
|
Betancur, Catalina
|
|
2002
|
70 |
5 |
p. 1381-1383
3 p.
|
artikel
|
| 22 |
Mapping of Gene Loci for Nephronophthisis Type 4 and Senior-Løken Syndrome, to Chromosome 1p36
|
Schuermann, Maria J.
|
|
2002
|
70 |
5 |
p. 1240-1246
7 p.
|
artikel
|
| 23 |
Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome
|
Richard, Gabriele
|
|
2002
|
70 |
5 |
p. 1341-1348
8 p.
|
artikel
|
| 24 |
PARK3 Influences Age at Onset in Parkinson Disease: A Genome Scan in the GenePD Study
|
DeStefano, Anita L.
|
|
2002
|
70 |
5 |
p. 1089-1095
7 p.
|
artikel
|
| 25 |
PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats
|
Onuchic, Luiz F.
|
|
2002
|
70 |
5 |
p. 1305-1317
13 p.
|
artikel
|
| 26 |
Quantitative-Trait Loci on Chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 Control Variation in Levels of T and B Lymphocyte Subpopulations
|
Hall, M.A.
|
|
2002
|
70 |
5 |
p. 1172-1182
11 p.
|
artikel
|
| 27 |
Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups
|
Herrnstadt, Corinna
|
|
2002
|
70 |
5 |
p. 1152-1171
20 p.
|
artikel
|
| 28 |
Reply to Tarazona-Santos and Santos
|
Lell, Jeffrey T.
|
|
2002
|
70 |
5 |
p. 1380-1381
2 p.
|
artikel
|
| 29 |
Revised 14.7-cM Locus for the Hyperparathyroidism–Jaw Tumor Syndrome Gene, HRPT2
|
Hobbs, Maurine R.
|
|
2002
|
70 |
5 |
p. 1376-1377
2 p.
|
artikel
|
| 30 |
Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, with Myotonic Myopathy and Chondrodysplasia
|
Arikawa-Hirasawa, Eri
|
|
2002
|
70 |
5 |
p. 1368-1375
8 p.
|
artikel
|
| 31 |
The Peopling of the Americas: A Second Major Migration?
|
Tarazona-Santos, Eduardo
|
|
2002
|
70 |
5 |
p. 1377-1380
4 p.
|
artikel
|
| 32 |
The TRIM37 Gene Encodes a Peroxisomal RING-B-Box-Coiled-Coil Protein: Classification of Mulibrey Nanism as a New Peroxisomal Disorder
|
Kallijärvi, Jukka
|
|
2002
|
70 |
5 |
p. 1215-1228
14 p.
|
artikel
|
| 33 |
This Month in the Journal
|
Beauregard, Kathryn
|
|
2002
|
70 |
5 |
p. i-ii
nvt p.
|
artikel
|
| 34 |
X-Linked Mental Retardation with Seizures and Carrier Manifestations Is Caused by a Mutation in the Creatine-Transporter Gene (SLC6A8) Located in Xq28
|
Hahn, Kimberly A.
|
|
2002
|
70 |
5 |
p. 1349-1356
8 p.
|
artikel
|
| 35 |
Y-Chromosomal DNA Variation in Pakistan
|
Qamar, Raheel
|
|
2002
|
70 |
5 |
p. 1107-1124
18 p.
|
artikel
|
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