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                             29 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A High-Density Admixture Map for Disease Gene Discovery in African Americans Smith, Michael W.
2004
74 5 p. 1001-1013
13 p.
artikel
2 Analyses of Genetic Structure of Tibeto-Burman Populations Reveals Sex-Biased Admixture in Southern Tibeto-Burmans Wen, Bo
2004
74 5 p. 856-865
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 Human Genetics, Emory University School of Medicine, 615 Michael Street, Room 301, 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. 2004
74 5 p. 1075-1079
5 p.
artikel
4 Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2 Li, Anren
2004
74 5 p. 817-826
10 p.
artikel
5 Ching Chun Li (1912–2003):A Personal Remembrance of a Hero of Genetics Chakravarti, Aravinda
2004
74 5 p. 789-792
4 p.
artikel
6 Design and Analysis of Admixture Mapping Studies Hoggart, C.J.
2004
74 5 p. 965-978
14 p.
artikel
7 Erratum 2004
74 5 p. 1080-
1 p.
artikel
8 Fragile-X–Associated Tremor/Ataxia Syndrome (FXTAS) in Females with the FMR1 Premutation Hagerman, R.J.
2004
74 5 p. 1051-1056
6 p.
artikel
9 Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and Finding of Significant Linkage to Chromosome 6q22 Middleton, F.A.
2004
74 5 p. 886-897
12 p.
artikel
10 Genomewide Linkage Scan Identifies a Novel Susceptibility Locus for Restless Legs Syndrome on Chromosome 9p Chen, Shenghan
2004
74 5 p. 876-885
10 p.
artikel
11 Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates Lafrenière, Ronald G.
2004
74 5 p. 1064-1073
10 p.
artikel
12 Inferring Phylogenies. Wooding, Stephen
2004
74 5 p. 1074-
1 p.
artikel
13 Linkage Disequilibrium Mapping of Schizophrenia Susceptibility to the CAPON Region of Chromosome 1q22 Brzustowicz, Linda M.
2004
74 5 p. 1057-1063
7 p.
artikel
14 Little Loss of Information Due to Unknown Phase for Fine-Scale Linkage-Disequilibrium Mapping with Single-Nucleotide–Polymorphism Genotype Data Morris, A.P.
2004
74 5 p. 945-953
9 p.
artikel
15 Methods for High-Density Admixture Mapping of Disease Genes Patterson, Nick
2004
74 5 p. 979-1000
22 p.
artikel
16 MSH2 c.1452–1455delAATG Is a Founder Mutation and an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Southern Chinese Population Chan, Tsun Leung
2004
74 5 p. 1035-1042
8 p.
artikel
17 Mutations in AXIN2 Cause Familial Tooth Agenesis and Predispose to Colorectal Cancer Lammi, Laura
2004
74 5 p. 1043-1050
8 p.
artikel
18 Myotonic Dystrophy: RNA Pathogenesis Comes into Focus Ranum, Laura P.W.
2004
74 5 p. 793-804
12 p.
artikel
19 Natural Selection and Population History in the Human Angiotensinogen Gene (AGT): 736 Complete AGT Sequences in Chromosomes from Around the World Nakajima, Toshiaki
2004
74 5 p. 898-916
19 p.
artikel
20 Novel PMS2 Pseudogenes Can Conceal Recessive Mutations Causing a Distinctive Childhood Cancer Syndrome De Vos, Michel
2004
74 5 p. 954-964
11 p.
artikel
21 Origin, Diffusion, and Differentiation of Y-Chromosome Haplogroups E and J: Inferences on the Neolithization of Europe and Later Migratory Events in the Mediterranean Area Semino, Ornella
2004
74 5 p. 1023-1034
12 p.
artikel
22 Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa Cruciani, Fulvio
2004
74 5 p. 1014-1022
9 p.
artikel
23 Polymorphisms in the Low-Density Lipoprotein Receptor–Related Protein 5 (LRP5) Gene Are Associated with Variation in Vertebral Bone Mass, Vertebral Bone Size, and Stature in Whites Ferrari, Serge L.
2004
74 5 p. 866-875
10 p.
artikel
24 Positional Cloning by Linkage Disequilibrium Maniatis, Nikolas
2004
74 5 p. 846-855
10 p.
artikel
25 Rare Autosomal Recessive Cardiac Valvular Form of Ehlers-Danlos Syndrome Results from Mutations in the COL1A2 Gene That Activate the Nonsense-Mediated RNA Decay Pathway Schwarze, Ulrike
2004
74 5 p. 917-930
14 p.
artikel
26 The Fragile-X Premutation: A Maturing Perspective Hagerman, Paul J.
2004
74 5 p. 805-816
12 p.
artikel
27 The Genetic Architecture of Selection at the Human Dopamine Receptor D4 (DRD4) Gene Locus Wang, E.
2004
74 5 p. 931-944
14 p.
artikel
28 This Month in the Journal Garber, Kathryn
2004
74 5 p. i-ii
nvt p.
artikel
29 Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor Quintana-Murci, Lluís
2004
74 5 p. 827-845
19 p.
artikel
                             29 gevonden resultaten
 
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