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                             34 results found
no title author magazine year volume issue page(s) type
1 A Genetic Factor for Age-Related Cataract: Identification and Characterization of a Novel Galactokinase Variant, “Osaka,” in Asians Okano, Yoshiyuki
 2001
 68 4 p. 1036-1042
7 p.
 article
2 A Genomewide Screen in Multiplex Rheumatoid Arthritis Families Suggests Genetic Overlap with Other Autoimmune Diseases Jawaheer, Damini
 2001
 68 4 p. 927-936
10 p.
 article
3 A New Statistical Method for Haplotype Reconstruction from Population Data Stephens, Matthew
 2001
 68 4 p. 978-989
12 p.
 article
4 An Extensive Analysis of Y-Chromosomal Microsatellite Haplotypes in Globally Dispersed Human Populations Kayser, Manfred
 2001
 68 4 p. 990-1018
29 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, Emory University School of Medicine, 1462 Clifton Road, Room B28, 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. 2001
 68 4 p. 1069-1074
6 p.
 article
6 A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy Escayg, Andrew
 2001
 68 4 p. 866-873
8 p.
 article
7 Assessment of Parent-of-Origin Effects in Linkage Analysis of Quantitative Traits Hanson, Robert L.
 2001
 68 4 p. 951-962
12 p.
 article
8 Axonemal Dynein Intermediate-Chain Gene (DNAI1) Mutations Result in Situs Inversus and Primary Ciliary Dyskinesia (Kartagener Syndrome) Guichard, Cécile
 2001
 68 4 p. 1030-1035
6 p.
 article
9 Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency Binzak, Barbara A.
 2001
 68 4 p. 839-847
9 p.
 article
10 Correcting for a Potential Bias in the Pedigree Disequilibrium Test Martin, Eden R.
 2001
 68 4 p. 1065-1067
3 p.
 article
11 Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome Petek, Erwin
 2001
 68 4 p. 848-858
11 p.
 article
12 Efficient Multipoint Linkage Analysis through Reduction of Inheritance Space Markianos, Kyriacos
 2001
 68 4 p. 963-977
15 p.
 article
13 Erratum 2001
 68 4 p. 1075-
1 p.
 article
14 Erratum 2001
 68 4 p. 1075-
1 p.
 article
15 Erratum 2001
 68 4 p. 1075-1076
2 p.
 article
16 Evaluation of Linkage and Association of HPC2/ELAC2 in Patients with Familial or Sporadic Prostate Cancer Xu, Jianfeng
 2001
 68 4 p. 901-911
11 p.
 article
17 High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula Bosch, Elena
 2001
 68 4 p. 1019-1029
11 p.
 article
18 Homozygosity Mapping Places the Acrodermatitis Enteropathica Gene on Chromosomal Region 8q24.3 Wang, Kun
 2001
 68 4 p. 1055-1060
6 p.
 article
19 HPC2 Variants and Screen-Detected Prostate Cancer Vesprini, Danny
 2001
 68 4 p. 912-917
6 p.
 article
20 Introductory Speech for F. Clarke Fraser * Warburton, Dorothy
 2001
 68 4 p. 826-827
2 p.
 article
21 Limitations of Chromosome Classification by Multicolor Karyotyping Lee, Charles
 2001
 68 4 p. 1043-1047
5 p.
 article
22 Linkage Analysis of a Complex Pedigree with Severe Bipolar Disorder, Using a Markov Chain Monte Carlo Method Garner, Chad
 2001
 68 4 p. 1061-1064
4 p.
 article
23 Localization of a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, PARK6, on Human Chromosome 1p35-p36 Valente, Enza Maria
 2001
 68 4 p. 895-900
6 p.
 article
24 Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red Hair Bastiaens, Maarten T.
 2001
 68 4 p. 884-894
11 p.
 article
25 Multipoint Linkage-Disequilibrium–Mapping Approach Based on the Case-Parent Trio Design Liang, Kung-Yee
 2001
 68 4 p. 937-950
14 p.
 article
26 Mutations of MLC1 (KIAA0027), Encoding a Putative Membrane Protein, Cause Megalencephalic Leukoencephalopathy with Subcortical Cysts Leegwater, Peter A.J.
 2001
 68 4 p. 831-838
8 p.
 article
27 Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus Wallace, R.H.
 2001
 68 4 p. 859-865
7 p.
 article
28 Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements Giglio, Sabrina
 2001
 68 4 p. 874-883
10 p.
 article
29 On Discovery, Genomes, The Society, and Society * Worton, Ronald G.
 2001
 68 4 p. 819-825
7 p.
 article
30 Principles of Molecular Oncology Jenkins, Robert
 2001
 68 4 p. 1068-
1 p.
 article
31 Resetting our Educational Sights: Unconstructing the Public's Dreams and Nightmares of the Genetic Revolution * Fraser, F. Clarke
 2001
 68 4 p. 828-830
3 p.
 article
32 Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7 Goobie, Sharan
 2001
 68 4 p. 1048-1054
7 p.
 article
33 This Month in the Journal Beauregard, Kathryn
 2001
 68 4 p. i-ii
nvt p.
 article
34 Whole-Genome Screening in Ankylosing Spondylitis: Evidence of Non-MHC Genetic-Susceptibility Loci Laval, S.H.
 2001
 68 4 p. 918-926
9 p.
 article
                             34 results found
 
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