| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter
|
Shohat, Mordechai
|
|
1997
|
61 |
5 |
p. 1139-1143
5 p.
|
artikel
|
| 2 |
Allele-Sharing Models: LOD Scores and Accurate Linkage Tests
|
Kong, Augustine
|
|
1997
|
61 |
5 |
p. 1179-1188
10 p.
|
artikel
|
| 3 |
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 Pathology, Box 357470, University of Washington, Seattle, WA 98195-7470, or fax them to (206) 685-9684. Submission must be received three full months 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 150 words, excluding the address for correspondence. Please include a cover letter indicating the name of the sponsoring ASHG member.
|
|
|
1997
|
61 |
5 |
p. 1210-1212
3 p.
|
artikel
|
| 4 |
CFTR Gene Mutations in Men with Bilateral Ejaculatory-Duct Obstruction and Anomalies of the Seminal Vesicles
|
Meschede, Dieter
|
|
1997
|
61 |
5 |
p. 1200-1202
3 p.
|
artikel
|
| 5 |
Childhood Cancer and Neural Tube Defects
|
Little, Julian
|
|
1997
|
61 |
5 |
p. 1204-1205
2 p.
|
artikel
|
| 6 |
D4 Dopamine-Receptor (DRD4) Alleles and Novelty Seeking in Substance-Dependent, Personality-Disorder, and Control Subjects
|
Gelernter, J.
|
|
1997
|
61 |
5 |
p. 1144-1152
9 p.
|
artikel
|
| 7 |
De Novo Rearrangements Found in 2% of Index Patients with Spinal Muscular Atrophy: Mutational Mechanisms, Parental Origin, Mutation Rate, and Implications for Genetic Counseling
|
Wirth, Brunhilde
|
|
1997
|
61 |
5 |
p. 1102-1111
10 p.
|
artikel
|
| 8 |
Detection of Gene-Environment Interactions in Joint Segregation and Linkage Analysis
|
Gauderman, W. James
|
|
1997
|
61 |
5 |
p. 1189-1199
11 p.
|
artikel
|
| 9 |
d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder
|
Suzuki, Yasuyuki
|
|
1997
|
61 |
5 |
p. 1153-1162
10 p.
|
artikel
|
| 10 |
DNA Variation and Language Affinities
|
Barbujani, Guido
|
|
1997
|
61 |
5 |
p. 1011-1014
4 p.
|
artikel
|
| 11 |
Effect of Genetic Heterogeneity and Assortative Mating on Linkage Analysis: A Simulation Study
|
Falk, Catherine T.
|
|
1997
|
61 |
5 |
p. 1169-1178
10 p.
|
artikel
|
| 12 |
Evidence for Locus Heterogeneity in Puerto Ricans with Hermansky-Pudlak Syndrome
|
Hazelwood, Senator
|
|
1997
|
61 |
5 |
p. 1088-1094
7 p.
|
artikel
|
| 13 |
Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele
|
McGee, T.L.
|
|
1997
|
61 |
5 |
p. 1059-1066
8 p.
|
artikel
|
| 14 |
Familial Multiple-System Tauopathy with Presenile Dementia Is Localized to Chromosome 17
|
Murrell, J.R.
|
|
1997
|
61 |
5 |
p. 1131-1138
8 p.
|
artikel
|
| 15 |
Familial Nontoxic Multinodular Thyroid Goiter Locus Maps to Chromosome 14q but Does Not Account for Familial Nonmedullary Thyroid Cancer
|
Bignell, Graham R.
|
|
1997
|
61 |
5 |
p. 1123-1130
8 p.
|
artikel
|
| 16 |
Genetic Linkage of Paget Disease of the Bone to Chromosome 18q
|
Cody, J.D.
|
|
1997
|
61 |
5 |
p. 1117-1122
6 p.
|
artikel
|
| 17 |
Human Genetic Affinities for Y-Chromosome P49a,f/TaqI Haplotypes Show Strong Correspondence with Linguistics
|
Poloni, E.S.
|
|
1997
|
61 |
5 |
p. 1015-1035
21 p.
|
artikel
|
| 18 |
Laboratory Policies and Practices for the Genetic Testing of Children: A Survey of the Helix Network
|
Wertz, Dorothy C.
|
|
1997
|
61 |
5 |
p. 1163-1168
6 p.
|
artikel
|
| 19 |
Lafora Progressive Myoclonus Epilepsy: Narrowing the Chromosome 6q24 Locus by Recombinations and Homozygosities
|
Sainz, Jesus
|
|
1997
|
61 |
5 |
p. 1205-1209
5 p.
|
artikel
|
| 20 |
Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search
|
Gasparini, P.
|
|
1997
|
61 |
5 |
p. 1112-1116
5 p.
|
artikel
|
| 21 |
Loss of Heterozygosity or: How I Learned to Stop Worrying and Love Mitotic Recombination
|
Tischfield, Jay A.
|
|
1997
|
61 |
5 |
p. 995-999
5 p.
|
artikel
|
| 22 |
“Mistakes Happen”: Somatic Mutation and Disease
|
Qian, Feng
|
|
1997
|
61 |
5 |
p. 1000-1005
6 p.
|
artikel
|
| 23 |
Molecular Analysis of the Androgen-Receptor Gene in a Family with Receptor-Positive Partial Androgen Insensitivity: An Unusual Type of Intronic Mutation
|
Brüggenwirth, H.T.
|
|
1997
|
61 |
5 |
p. 1067-1077
11 p.
|
artikel
|
| 24 |
Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome
|
Johnston, Jennifer
|
|
1997
|
61 |
5 |
p. 1053-1058
6 p.
|
artikel
|
| 25 |
Mutation Detection in the Repeated Part of the PKD1 Gene
|
Roelfsema, Jeroen H.
|
|
1997
|
61 |
5 |
p. 1044-1052
9 p.
|
artikel
|
| 26 |
Mutations in the TIGR Gene in Familial Primary Open-Angle Glaucoma in Japan
|
Suzuki, Yasuyuki
|
|
1997
|
61 |
5 |
p. 1202-1204
3 p.
|
artikel
|
| 27 |
Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene
|
Yue, Qing
|
|
1997
|
61 |
5 |
p. 1078-1087
10 p.
|
artikel
|
| 28 |
Reply to Little
|
Narod, Steven
|
|
1997
|
61 |
5 |
p. 1205-
1 p.
|
artikel
|
| 29 |
Rufous Oculocutaneous Albinism in Southern African Blacks Is Caused by Mutations in the TYRP1 Gene
|
Manga, P.
|
|
1997
|
61 |
5 |
p. 1095-1101
7 p.
|
artikel
|
| 30 |
The Role of MMAC1 Mutations in Early-Onset Breast Cancer: Causative in Association with Cowden Syndrome and Excluded in BRCA1-Negative Cases
|
Tsou, Hui C.
|
|
1997
|
61 |
5 |
p. 1036-1043
8 p.
|
artikel
|
| 31 |
This Month in the Journal
|
Ashkenas, John
|
|
1997
|
61 |
5 |
p. i-ii
nvt p.
|
artikel
|
| 32 |
Understanding Human Cancer in a Fly?
|
St. John, Maie A.R.
|
|
1997
|
61 |
5 |
p. 1006-1010
5 p.
|
artikel
|
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