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                             40 results found
no title author magazine year volume issue page(s) type
1 A Generalization of the Transmission/Disequilibrium Test for Uncertain-Haplotype Transmission Clayton, David
1999
65 4 p. 1170-1177
8 p.
article
2 A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci Hovatta, Iiris
1999
65 4 p. 1114-1124
11 p.
article
3 A Missense Mutation of Cytochrome Oxidase Subunit II Causes Defective Assembly and Myopathy Rahman, Shamima
1999
65 4 p. 1030-1039
10 p.
article
4 An Empirical Exploration of the (Δμ)2 Genetic Distance for 213 Human Microsatellite Markers Cooper, Gillian
1999
65 4 p. 1125-1133
9 p.
article
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 Pathology, Box 357470, University of Washington, Seattle, WA 98195-7470; fax them to (206) 685-9684; or send via E-mail to ajhg@u.washington.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. 1999
65 4 p. 1211-1213
3 p.
article
6 A Novel Syndrome of Episodic Muscle Weakness Maps to Xp22.3 Ryan, Monique M.
1999
65 4 p. 1104-1113
10 p.
article
7 Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors Varley, Jennifer M.
1999
65 4 p. 995-1006
12 p.
article
8 A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33 Baulac, Stéphanie
1999
65 4 p. 1078-1085
8 p.
article
9 Assignment of the Locus for Hydrolethalus Syndrome to a Highly Restricted Region on 11q23-25 Visapää, Ilona
1999
65 4 p. 1086-1095
10 p.
article
10 Chinese Geneticists Are Far from Eugenics Movement Chen, Zhu
1999
65 4 p. 1199-
1 p.
article
11 Cultural Difference and the Eugenics Law Guo, Sun-Wei
1999
65 4 p. 1197-1199
3 p.
article
12 Cysteine Substitutions in Epidermal Growth Factor–Like Domains of Fibrillin-1: Distinct Effects on Biochemical and Clinical Phenotypes Schrijver, I.
1999
65 4 p. 1007-1020
14 p.
article
13 Distribution of Two HIV-1–Resistant Polymorphisms (SDF1-3′A and CCR2-64I) in East Asian and World Populations and Its Implication in AIDS Epidemiology Su, Bing
1999
65 4 p. 1047-1053
7 p.
article
14 Errata 1999
65 4 p. 1214-
1 p.
article
15 Errata 1999
65 4 p. 1214-
1 p.
article
16 Genes, Demography, and Life Span: The Contribution of Demographic Data in Genetic Studies on Aging and Longevity Yashin, A.I.
1999
65 4 p. 1178-1193
16 p.
article
17 Genetic Linkage of the Muckle-Wells Syndrome to Chromosome 1q44 Cuisset, Laurence
1999
65 4 p. 1054-1059
6 p.
article
18 Genome Scan for Predisposing Loci for Distal Interphalangeal Joint Osteoarthritis: Evidence for a Locus on 2q Leppävuori, Jenni
1999
65 4 p. 1060-1067
8 p.
article
19 Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22 Jung, Martin
1999
65 4 p. 1068-1077
10 p.
article
20 Joint Multipoint Linkage Analysis of Multivariate Qualitative and Quantitative Traits. II. Alcoholism and Event-Related Potentials Williams, Jeff T.
1999
65 4 p. 1148-1160
13 p.
article
21 Joint Multipoint Linkage Analysis of Multivariate Qualitative and Quantitative Traits. I. Likelihood Formulation and Simulation Results Williams, Jeff T.
1999
65 4 p. 1134-1147
14 p.
article
22 Kallmann Syndrome and the Link between Olfactory and Reproductive Development Rugarli, Elena I.
1999
65 4 p. 943-948
6 p.
article
23 Linkage of Familial Schizophrenia to Chromosome 13q32 Brzustowicz, Linda M.
1999
65 4 p. 1096-1103
8 p.
article
24 Naturally Occurring Mutations of the Luteinizing-Hormone Receptor: Lessons Learned about Reproductive Physiology and G Protein–Coupled Receptors Latronico, Ana Claudia
1999
65 4 p. 949-958
10 p.
article
25 New Solutions to an Ancient Riddle: Defining the Differences between Adam and Eve Roberts, Lori M.
1999
65 4 p. 933-942
10 p.
article
26 Reply to Guo and to Chen et al. Mao, Xin
1999
65 4 p. 1199-1201
3 p.
article
27 Reply to Michie and Marteau Middleton, A.
1999
65 4 p. 1207-1208
2 p.
article
28 Reply to Sharpe Fitzpatrick, Jennifer L.
1999
65 4 p. 1204-
1 p.
article
29 SPERMSEG: Analysis of Segregation Distortion in Single-Sperm Data McPeek, Mary Sara
1999
65 4 p. 1195-1197
3 p.
article
30 Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes Annunen, Susanna
1999
65 4 p. 974-983
10 p.
article
31 STAT5 Signaling in Sexually Dimorphic Gene Expression and Growth Patterns Davey, Helen W.
1999
65 4 p. 959-965
7 p.
article
32 Temperature-Sensitive RB Mutations Linked to Incomplete Penetrance of Familial Retinoblastoma in 12 Families Otterson, Gregory A.
1999
65 4 p. 1040-1046
7 p.
article
33 The Choice to Have a Disabled Child Michie, Susan
1999
65 4 p. 1204-1207
4 p.
article
34 The Contribution of Germline BRCA1 and BRCA2 Mutations to Familial Ovarian Cancer: No Evidence for Other Ovarian Cancer–Susceptibility Genes Gayther, Simon A.
1999
65 4 p. 1021-1029
9 p.
article
35 The Duty to Recontact: Benefit and Harm Sharpe, Neil F.
1999
65 4 p. 1201-1204
4 p.
article
36 This Month in the Journal Ashkenas, John
1999
65 4 p. i-ii
nvt p.
article
37 Tissue-Specific Somatic Mosaicism in Spinal and Bulbar Muscular Atrophy Is Dependent on CAG-Repeat Length and Androgen Receptor–Gene Expression Level Tanaka, Fumiaki
1999
65 4 p. 966-973
8 p.
article
38 Transmission/Disequilibrium Tests for Extended Marker Haplotypes Clayton, David
1999
65 4 p. 1161-1169
9 p.
article
39 Using Exact P Values to Compare the Power between the Reconstruction-Combined Transmission/Disequilibrium Test and the Sib Transmission/Disequilibrium Test Knapp, Michael
1999
65 4 p. 1208-1210
3 p.
article
40 Variegate Porphyria in Western Europe: Identification of PPOX Gene Mutations in 104 Families, Extent of Allelic Heterogeneity, and Absence of Correlation between Phenotype and Type of Mutation Whatley, Sharon D.
1999
65 4 p. 984-994
11 p.
article
                             40 results found
 
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