| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A 3.9-Centimorgan-Resolution Human Single-Nucleotide Polymorphism Linkage Map and Screening Set
|
Matise, Tara C.
|
|
2003
|
73 |
2 |
p. 271-284
14 p.
|
artikel
|
| 2 |
African American Hypertensive Nephropathy Maps to a New Locus on Chromosome 9q31-q32
|
Chung, Ki Wha
|
|
2003
|
73 |
2 |
p. 420-429
10 p.
|
artikel
|
| 3 |
A Gene Locus Responsible for Dyschromatosis Symmetrica Hereditaria (DSH) Maps to Chromosome 6q24.2-q25.2
|
Xing, Qing-he
|
|
2003
|
73 |
2 |
p. 377-382
6 p.
|
artikel
|
| 4 |
A New Familial Amyotrophic Lateral Sclerosis Locus on Chromosome 16q12.1-16q12.2
|
Abalkhail, Halah
|
|
2003
|
73 |
2 |
p. 383-389
7 p.
|
artikel
|
| 5 |
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
|
73 |
2 |
p. 442-443
2 p.
|
artikel
|
| 6 |
BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy
|
Pal, Deb K.
|
|
2003
|
73 |
2 |
p. 261-270
10 p.
|
artikel
|
| 7 |
Discordance between Genetic and Epigenetic Defects in Pseudohypoparathyroidism Type 1b Revealed by Inconsistent Loss of Maternal Imprinting at GNAS1
|
Jan de Beur, Suzanne
|
|
2003
|
73 |
2 |
p. 314-322
9 p.
|
artikel
|
| 8 |
Erratum
|
|
|
2003
|
73 |
2 |
p. 445-
1 p.
|
artikel
|
| 9 |
Erratum
|
|
|
2003
|
73 |
2 |
p. 445-
1 p.
|
artikel
|
| 10 |
Finding Haplotype Block Boundaries by Using the Minimum-Description-Length Principle
|
Anderson, Eric C.
|
|
2003
|
73 |
2 |
p. 336-354
19 p.
|
artikel
|
| 11 |
Germline PTEN Promoter Mutations and Deletions in Cowden/Bannayan-Riley-Ruvalcaba Syndrome Result in Aberrant PTEN Protein and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pathway
|
Zhou, Xiao-Ping
|
|
2003
|
73 |
2 |
p. 404-411
8 p.
|
artikel
|
| 12 |
Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis
|
Sapp, Peter C.
|
|
2003
|
73 |
2 |
p. 397-403
7 p.
|
artikel
|
| 13 |
Linkage Disequilibrium and Inference of Ancestral Recombination in 538 Single-Nucleotide Polymorphism Clusters across the Human Genome
|
Clark, Andrew G.
|
|
2003
|
73 |
2 |
p. 285-300
16 p.
|
artikel
|
| 14 |
Localization of a Novel Melanoma Susceptibility Locus to 1p22
|
Gillanders, Elizabeth
|
|
2003
|
73 |
2 |
p. 301-313
13 p.
|
artikel
|
| 15 |
Localization of a Susceptibility Gene for Type 2 Diabetes to Chromosome 5q34–q35.2
|
Reynisdottir, Inga
|
|
2003
|
73 |
2 |
p. 323-335
13 p.
|
artikel
|
| 16 |
Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation
|
Matsumoto, Naomi
|
|
2003
|
73 |
2 |
p. 233-246
14 p.
|
artikel
|
| 17 |
Mutations of von Hippel-Lindau Tumor-Suppressor Gene and Congenital Polycythemia
|
Pastore, Yves
|
|
2003
|
73 |
2 |
p. 412-419
8 p.
|
artikel
|
| 18 |
New Molecular Mechanism for Ullrich Congenital Muscular Dystrophy: A Heterozygous In-Frame Deletion in the COL6A1 Gene Causes a Severe Phenotype
|
Pan, Te-Cheng
|
|
2003
|
73 |
2 |
p. 355-369
15 p.
|
artikel
|
| 19 |
Notice of Retraction
|
Warren, Stephen T.
|
|
2003
|
73 |
2 |
p. 444-
1 p.
|
artikel
|
| 20 |
Nuclear and Mitochondrial DNA Analysis of a 2,000-Year-Old Necropolis in the Egyin Gol Valley of Mongolia
|
Keyser-Tracqui, Christine
|
|
2003
|
73 |
2 |
p. 247-260
14 p.
|
artikel
|
| 21 |
Selection in the Ashkenazi Jewish Population Unlikely—Reply to Zlotogora and Bach
|
Risch, Neil
|
|
2003
|
73 |
2 |
p. 440-441
2 p.
|
artikel
|
| 22 |
Sequence Variants of the Brain-Derived Neurotrophic Factor (BDNF) Gene Are Strongly Associated with Obsessive-Compulsive Disorder
|
Hall, Diana
|
|
2003
|
73 |
2 |
p. 370-376
7 p.
|
artikel
|
| 23 |
The International Psoriasis Genetics Study: Assessing Linkage to 14 Candidate Susceptibility Loci in a Cohort of 942 Affected Sib Pairs
|
|
|
2003
|
73 |
2 |
p. 430-437
8 p.
|
artikel
|
| 24 |
The Possibility of a Selection Process in the Ashkenazi Jewish Population
|
Zlotogora, Joel
|
|
2003
|
73 |
2 |
p. 438-440
3 p.
|
artikel
|
| 25 |
This Month in the Journal
|
Garber, Kathryn
|
|
2003
|
73 |
2 |
p. i-ii
nvt p.
|
artikel
|
| 26 |
Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16q
|
Ruddy, Deborah M.
|
|
2003
|
73 |
2 |
p. 390-396
7 p.
|
artikel
|
| 27 |
Two-Locus Heterogeneity Cannot Be Distinguished from Two-Locus Epistasis on the Basis of Affected-Sib-Pair Data
|
Vieland, Veronica J.
|
|
2003
|
73 |
2 |
p. 223-232
10 p.
|
artikel
|
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