| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain
|
Bray, Nicholas J.
|
|
2003
|
73 |
1 |
p. 152-161
10 p.
|
artikel
|
| 2 |
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 |
1 |
p. 221-222
2 p.
|
artikel
|
| 3 |
Babyface: A Story of Heart and Bones
|
Acheson, Louise
|
|
2003
|
73 |
1 |
p. 219-220
2 p.
|
artikel
|
| 4 |
Crossover Interference in Humans
|
Housworth, E.A.
|
|
2003
|
73 |
1 |
p. 188-197
10 p.
|
artikel
|
| 5 |
DNA Microarrays: A Molecular Cloning Manual
|
Lagarde, Alain E.
|
|
2003
|
73 |
1 |
p. 218-219
2 p.
|
artikel
|
| 6 |
Ehlers-Danlos Syndrome with Severe Early-Onset Periodontal Disease (EDS-VIII) Is a Distinct, Heterogeneous Disorder with One Predisposition Gene at Chromosome 12p13
|
Rahman, Nazneen
|
|
2003
|
73 |
1 |
p. 198-204
7 p.
|
artikel
|
| 7 |
Expressivity of Holt-Oram Syndrome Is Not Predicted by TBX5 Genotype
|
Brassington, Anna-Marie E.
|
|
2003
|
73 |
1 |
p. 74-85
12 p.
|
artikel
|
| 8 |
Fabry Disease: Novel α-Galactosidase A 3′-Terminal Mutations Result in Multiple Transcripts Due to Aberrant 3′-End Formation
|
Yasuda, Makiko
|
|
2003
|
73 |
1 |
p. 162-173
12 p.
|
artikel
|
| 9 |
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder
|
Segurado, Ricardo
|
|
2003
|
73 |
1 |
p. 49-62
14 p.
|
artikel
|
| 10 |
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
|
Lewis, Cathryn M.
|
|
2003
|
73 |
1 |
p. 34-48
15 p.
|
artikel
|
| 11 |
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part I: Methods and Power Analysis
|
Levinson, Douglas F.
|
|
2003
|
73 |
1 |
p. 17-33
17 p.
|
artikel
|
| 12 |
Genomewide Linkage Analyses of Bipolar Disorder: A New Sample of 250 Pedigrees from the National Institute of Mental Health Genetics Initiative
|
Dick, Danielle M.
|
|
2003
|
73 |
1 |
p. 107-114
8 p.
|
artikel
|
| 13 |
Haploinsufficiency of TNXB Is Associated with Hypermobility Type of Ehlers-Danlos Syndrome
|
Zweers, Manon C.
|
|
2003
|
73 |
1 |
p. 214-217
4 p.
|
artikel
|
| 14 |
Haplotype Block Partition with Limited Resources and Applications to Human Chromosome 21 Haplotype Data
|
Zhang, Kui
|
|
2003
|
73 |
1 |
p. 63-73
11 p.
|
artikel
|
| 15 |
Hot and Cold Spots of Recombination in the Human Genome: the Reason We Should Find Them and How This Can Be Achieved
|
Arnheim, Norman
|
|
2003
|
73 |
1 |
p. 5-16
12 p.
|
artikel
|
| 16 |
IBD5 is a General Risk Factor for Inflammatory Bowel Disease: Replication of Association with Crohn Disease and Identification of a Novel Association with Ulcerative Colitis
|
Giallourakis, Cosmas
|
|
2003
|
73 |
1 |
p. 205-211
7 p.
|
artikel
|
| 17 |
Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin–Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome
|
Siegel, Dawn H.
|
|
2003
|
73 |
1 |
p. 174-187
14 p.
|
artikel
|
| 18 |
Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries
|
Mannila, H.
|
|
2003
|
73 |
1 |
p. 86-94
9 p.
|
artikel
|
| 19 |
Mutational Mechanisms of Williams-Beuren Syndrome Deletions
|
Bayés, Mònica
|
|
2003
|
73 |
1 |
p. 131-151
21 p.
|
artikel
|
| 20 |
Mutations in the Fumarate Hydratase Gene Cause Hereditary Leiomyomatosis and Renal Cell Cancer in Families in North America
|
Toro, Jorge R.
|
|
2003
|
73 |
1 |
p. 95-106
12 p.
|
artikel
|
| 21 |
Mutations in TNNT3 Cause Multiple Congenital Contractures: A Second Locus for Distal Arthrogryposis Type 2B
|
Sung, Sandy S.
|
|
2003
|
73 |
1 |
p. 212-214
3 p.
|
artikel
|
| 22 |
Selection of Genetic Markers for Association Analyses, Using Linkage Disequilibrium and Haplotypes
|
Meng, Zhaoling
|
|
2003
|
73 |
1 |
p. 115-130
16 p.
|
artikel
|
| 23 |
Sheldon C. Reed, Ph.D. (November 7, 1910–February 1, 2003): Genetic Counseling, Behavioral Genetics
|
Anderson, V. Elving
|
|
2003
|
73 |
1 |
p. 1-4
4 p.
|
artikel
|
| 24 |
This Month in the Journal
|
Garber, Kathryn
|
|
2003
|
73 |
1 |
p. i-ii
nvt p.
|
artikel
|
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