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                             32 results found
no title author magazine year volume issue page(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.
 article
2 Allele-Sharing Models: LOD Scores and Accurate Linkage Tests Kong, Augustine
 1997
 61 5 p. 1179-1188
10 p.
 article
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.
 article
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.
 article
5 Childhood Cancer and Neural Tube Defects Little, Julian
 1997
 61 5 p. 1204-1205
2 p.
 article
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.
 article
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.
 article
8 Detection of Gene-Environment Interactions in Joint Segregation and Linkage Analysis Gauderman, W. James
 1997
 61 5 p. 1189-1199
11 p.
 article
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.
 article
10 DNA Variation and Language Affinities Barbujani, Guido
 1997
 61 5 p. 1011-1014
4 p.
 article
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.
 article
12 Evidence for Locus Heterogeneity in Puerto Ricans with Hermansky-Pudlak Syndrome Hazelwood, Senator
 1997
 61 5 p. 1088-1094
7 p.
 article
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.
 article
14 Familial Multiple-System Tauopathy with Presenile Dementia Is Localized to Chromosome 17 Murrell, J.R.
 1997
 61 5 p. 1131-1138
8 p.
 article
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.
 article
16 Genetic Linkage of Paget Disease of the Bone to Chromosome 18q Cody, J.D.
 1997
 61 5 p. 1117-1122
6 p.
 article
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.
 article
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.
 article
19 Lafora Progressive Myoclonus Epilepsy: Narrowing the Chromosome 6q24 Locus by Recombinations and Homozygosities Sainz, Jesus
 1997
 61 5 p. 1205-1209
5 p.
 article
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.
 article
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.
 article
22 “Mistakes Happen”: Somatic Mutation and Disease Qian, Feng
 1997
 61 5 p. 1000-1005
6 p.
 article
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.
 article
24 Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome Johnston, Jennifer
 1997
 61 5 p. 1053-1058
6 p.
 article
25 Mutation Detection in the Repeated Part of the PKD1 Gene Roelfsema, Jeroen H.
 1997
 61 5 p. 1044-1052
9 p.
 article
26 Mutations in the TIGR Gene in Familial Primary Open-Angle Glaucoma in Japan Suzuki, Yasuyuki
 1997
 61 5 p. 1202-1204
3 p.
 article
27 Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene Yue, Qing
 1997
 61 5 p. 1078-1087
10 p.
 article
28 Reply to Little Narod, Steven
 1997
 61 5 p. 1205-
1 p.
 article
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.
 article
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.
 article
31 This Month in the Journal Ashkenas, John
 1997
 61 5 p. i-ii
nvt p.
 article
32 Understanding Human Cancer in a Fly? St. John, Maie A.R.
 1997
 61 5 p. 1006-1010
5 p.
 article
                             32 results found
 
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