| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of Age Effect on Meiotic Recombination between Human X and Y Chromosomes
|
Shi, Qinghua
|
|
2002
|
71 |
2 |
p. 254-261
8 p.
|
artikel
|
| 2 |
A CHEK2 Genetic Variant Contributing to a Substantial Fraction of Familial Breast Cancer
|
Vahteristo, Pia
|
|
2002
|
71 |
2 |
p. 432-438
7 p.
|
artikel
|
| 3 |
A Comprehensive Analysis of Recently Integrated Human Ta L1 Elements
|
Myers, Jeremy S.
|
|
2002
|
71 |
2 |
p. 312-326
15 p.
|
artikel
|
| 4 |
A Genetic Locus for Adolescent Idiopathic Scoliosis Linked to Chromosome 19p13.3
|
Chan, Vivian
|
|
2002
|
71 |
2 |
p. 401-406
6 p.
|
artikel
|
| 5 |
Analysis of Mitochondrial DNA Diversity in the Aleuts of the Commander Islands and Its Implications for the Genetic History of Beringia
|
Derbeneva, Olga A.
|
|
2002
|
71 |
2 |
p. 415-421
7 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 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
|
71 |
2 |
p. 445-447
3 p.
|
artikel
|
| 7 |
A Note on the Calculation of Empirical P Values from Monte Carlo Procedures
|
North, B.V.
|
|
2002
|
71 |
2 |
p. 439-441
3 p.
|
artikel
|
| 8 |
Atypical 5′ Splice Sites Cause CFTR Exon 9 To Be Vulnerable to Skipping
|
Hefferon, Timothy W.
|
|
2002
|
71 |
2 |
p. 294-303
10 p.
|
artikel
|
| 9 |
CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness
|
Astuto, L.M.
|
|
2002
|
71 |
2 |
p. 262-275
14 p.
|
artikel
|
| 10 |
Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization
|
White, Stefan
|
|
2002
|
71 |
2 |
p. 365-374
10 p.
|
artikel
|
| 11 |
Erratum
|
|
|
2002
|
71 |
2 |
p. 448-
1 p.
|
artikel
|
| 12 |
Erratum
|
|
|
2002
|
71 |
2 |
p. 449-
1 p.
|
artikel
|
| 13 |
Erratum
|
|
|
2002
|
71 |
2 |
p. 448-
1 p.
|
artikel
|
| 14 |
Evidence Consistent with Human L1 Retrotransposition in Maternal Meiosis I
|
Brouha, Brook
|
|
2002
|
71 |
2 |
p. 327-336
10 p.
|
artikel
|
| 15 |
Evidence that Griscelli Syndrome with Neurological Involvement Is Caused by Mutations in RAB27A, Not MYO5A
|
Anikster, Yair
|
|
2002
|
71 |
2 |
p. 407-414
8 p.
|
artikel
|
| 16 |
Genetic Isolates in East Asia: A Study of Linkage Disequilibrium in the X Chromosome
|
Katoh, T.
|
|
2002
|
71 |
2 |
p. 395-400
6 p.
|
artikel
|
| 17 |
Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia
|
Straub, Richard E.
|
|
2002
|
71 |
2 |
p. 337-348
12 p.
|
artikel
|
| 18 |
Genome Scan for Loci Involved in Cleft Lip With or Without Cleft Palate, in Chinese Multiplex Families
|
Marazita, Mary L.
|
|
2002
|
71 |
2 |
p. 349-364
16 p.
|
artikel
|
| 19 |
Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene
|
Digilio, Maria Cristina
|
|
2002
|
71 |
2 |
p. 389-394
6 p.
|
artikel
|
| 20 |
Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation
|
Giglio, Sabrina
|
|
2002
|
71 |
2 |
p. 276-285
10 p.
|
artikel
|
| 21 |
Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C
|
Novelli, Giuseppe
|
|
2002
|
71 |
2 |
p. 426-431
6 p.
|
artikel
|
| 22 |
Molecular Characterization of the Pericentric Inversion That Causes Differences Between Chimpanzee Chromosome 19 and Human Chromosome 17
|
Kehrer-Sawatzki, Hildegard
|
|
2002
|
71 |
2 |
p. 375-388
14 p.
|
artikel
|
| 23 |
Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia
|
Kohl, Susanne
|
|
2002
|
71 |
2 |
p. 422-425
4 p.
|
artikel
|
| 24 |
Powerful Regression-Based Quantitative-Trait Linkage Analysis of General Pedigrees
|
Sham, Pak C.
|
|
2002
|
71 |
2 |
p. 238-253
16 p.
|
artikel
|
| 25 |
Premature Termination Mutations in FBN1: Distinct Effects on Differential Allelic Expression and on Protein and Clinical Phenotypes
|
Schrijver, Iris
|
|
2002
|
71 |
2 |
p. 223-237
15 p.
|
artikel
|
| 26 |
Regression-Based Quantitative-Trait–Locus Mapping in the 21st Century
|
Feingold, Eleanor
|
|
2002
|
71 |
2 |
p. 217-222
6 p.
|
artikel
|
| 27 |
Response to Epstein et al.
|
Burton, Paul R.
|
|
2002
|
71 |
2 |
p. 441-442
2 p.
|
artikel
|
| 28 |
SNPs at the 3′ End of the Angiotensinogen Gene Define Two Haplotypes Associated with the Common 235Met Variant
|
Plummer, S.
|
|
2002
|
71 |
2 |
p. 443-444
2 p.
|
artikel
|
| 29 |
Species Differences in TSIX/Tsix Reveal the Roles of These Genes in X-Chromosome Inactivation
|
Migeon, Barbara R.
|
|
2002
|
71 |
2 |
p. 286-293
8 p.
|
artikel
|
| 30 |
Testing for Population Subdivision and Association in Four Case-Control Studies
|
Ardlie, Kristin G.
|
|
2002
|
71 |
2 |
p. 304-311
8 p.
|
artikel
|
| 31 |
This Month in the Journal
|
Beauregard, Kathryn
|
|
2002
|
71 |
2 |
p. i-ii
nvt p.
|
artikel
|
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