| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Genomewide Linkage Study of 1,933 Families Affected by Premature Coronary Artery Disease: The British Heart Foundation (BHF) Family Heart Study
|
|
|
2005
|
77 |
6 |
p. 1011-1020
10 p.
|
artikel
|
| 2 |
A Homozygous Missense Mutation in TGM5 Abolishes Epidermal Transglutaminase 5 Activity and Causes Acral Peeling Skin Syndrome
|
Cassidy, Andrew J.
|
|
2005
|
77 |
6 |
p. 909-917
9 p.
|
artikel
|
| 3 |
Announcements 1 1 Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to ajhg@ajhg.net. 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.
|
|
|
2005
|
77 |
6 |
p. 1132-1135
4 p.
|
artikel
|
| 4 |
Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios
|
Fallin, M. Daniele
|
|
2005
|
77 |
6 |
p. 918-936
19 p.
|
artikel
|
| 5 |
Comparative Genomics and Gene Expression Analysis Identifies BBS9, a New Bardet-Biedl Syndrome Gene
|
Nishimura, Darryl Y.
|
|
2005
|
77 |
6 |
p. 1021-1033
13 p.
|
artikel
|
| 6 |
Discriminating Power of Localized Three-Dimensional Facial Morphology
|
Hammond, Peter
|
|
2005
|
77 |
6 |
p. 999-1010
12 p.
|
artikel
|
| 7 |
Editorial Reviewers for 2005
|
|
|
2005
|
77 |
6 |
p. 904-908
5 p.
|
artikel
|
| 8 |
Erratum
|
|
|
2005
|
77 |
6 |
p. 1131-
1 p.
|
artikel
|
| 9 |
Genetic Testing for Cancer: Psychological Approaches for Helping Patients and Families.
|
Nedelcu, MS, CGC, Raluca
|
|
2005
|
77 |
6 |
p. 1130-
1 p.
|
artikel
|
| 10 |
Genomewide High-Density SNP Linkage Analysis of 236 Japanese Families Supports the Existence of Schizophrenia Susceptibility Loci on Chromosomes 1p, 14q, and 20p
|
Arinami, Tadao
|
|
2005
|
77 |
6 |
p. 937-944
8 p.
|
artikel
|
| 11 |
Genomewide Scan and Fine-Mapping Linkage Studies in Four European Samples with Bipolar Affective Disorder Suggest a New Susceptibility Locus on Chromosome 1p35-p36 and Provides Further Evidence of Loci on Chromosome 4q31 and 6q24
|
Schumacher, Johannes
|
|
2005
|
77 |
6 |
p. 1102-1111
10 p.
|
artikel
|
| 12 |
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
|
Snoeckx, Rikkert L.
|
|
2005
|
77 |
6 |
p. 945-957
13 p.
|
artikel
|
| 13 |
Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination
|
Woodward, Karen J.
|
|
2005
|
77 |
6 |
p. 966-987
22 p.
|
artikel
|
| 14 |
Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder
|
Hudson, Gavin
|
|
2005
|
77 |
6 |
p. 1086-1091
6 p.
|
artikel
|
| 15 |
Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation
|
Schüle, Birgitt
|
|
2005
|
77 |
6 |
p. 1117-1128
12 p.
|
artikel
|
| 16 |
Letter from the Editor
|
Warren, Steve
|
|
2005
|
77 |
6 |
p. 903-
1 p.
|
artikel
|
| 17 |
NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
|
De Luca, Alessandro
|
|
2005
|
77 |
6 |
p. 1092-1101
10 p.
|
artikel
|
| 18 |
Preferential Transmission of Paternal Alleles at Risk Genes in Attention-Deficit/Hyperactivity Disorder
|
Hawi, Ziarih
|
|
2005
|
77 |
6 |
p. 958-965
8 p.
|
artikel
|
| 19 |
Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia
|
Xue, Yali
|
|
2005
|
77 |
6 |
p. 1112-1116
5 p.
|
artikel
|
| 20 |
Replication of Putative Candidate-Gene Associations with Rheumatoid Arthritis in >4,000 Samples from North America and Sweden: Association of Susceptibility with PTPN22, CTLA4, and PADI4
|
Plenge, Robert M.
|
|
2005
|
77 |
6 |
p. 1044-1060
17 p.
|
artikel
|
| 21 |
Robust Estimation of Experimentwise P Values Applied to a Genome Scan of Multiple Asthma Traits Identifies a New Region of Significant Linkage on Chromosome 20q13
|
Ferreira, Manuel A.R.
|
|
2005
|
77 |
6 |
p. 1075-1085
11 p.
|
artikel
|
| 22 |
The Effect of Single-Nucleotide Polymorphism Marker Selection on Patterns of Haplotype Blocks and Haplotype Frequency Estimates
|
Nothnagel, Michael
|
|
2005
|
77 |
6 |
p. 988-998
11 p.
|
artikel
|
| 23 |
The Role of Mannosylated Enzyme and the Mannose Receptor in Enzyme Replacement Therapy
|
Du, Hong
|
|
2005
|
77 |
6 |
p. 1061-1074
14 p.
|
artikel
|
| 24 |
The Y Deletion gr/gr and Susceptibility to Testicular Germ Cell Tumor
|
Nathanson, Katherine L.
|
|
2005
|
77 |
6 |
p. 1034-1043
10 p.
|
artikel
|
| 25 |
This Month in the Journal
|
Garber, Kathryn
|
|
2005
|
77 |
6 |
p. i-ii
nvt p.
|
artikel
|
| 26 |
Velo-cardio-facial Syndrome: A Model for Understanding Microdeletion Disorders.
|
Robin, Nathaniel H.
|
|
2005
|
77 |
6 |
p. 1129-1130
2 p.
|
artikel
|
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