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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Functional Polymorphism in COL11A1, Which Encodes the α1 Chain of Type XI Collagen, Is Associated with Susceptibility to Lumbar Disc Herniation Mio, Futoshi
2007
81 6 p. 1271-1277
7 p.
artikel
2 A Genomewide Association Study of Skin Pigmentation in a South Asian Population Stokowski, Renee P.
2007
81 6 p. 1119-1132
14 p.
artikel
3 Announcements 1 1.  Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to ajhg@ajhg.net. 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. 2007
81 6 p. 1321-1323
3 p.
artikel
4 Common Single-Nucleotide Polymorphisms Act in Concert to Affect Plasma Levels of High-Density Lipoprotein Cholesterol Spirin, Victor
2007
81 6 p. 1298-1303
6 p.
artikel
5 Contribution of SHANK3 Mutations to Autism Spectrum Disorder Moessner, Rainald
2007
81 6 p. 1289-1297
9 p.
artikel
6 Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4 Bondurand, Nadege
2007
81 6 p. 1169-1185
17 p.
artikel
7 DNA Methylation Signatures within the Human Brain Ladd-Acosta, Christine
2007
81 6 p. 1304-1315
12 p.
artikel
8 Editorial Reviewers for 2007 2007
81 6 p. 1316-1320
5 p.
artikel
9 Genetic Basis for Correction of Very-Long-Chain Acyl–Coenzyme A Dehydrogenase Deficiency by Bezafibrate in Patient Fibroblasts: Toward a Genotype-Based Therapy Gobin-Limballe, S.
2007
81 6 p. 1133-1143
11 p.
artikel
10 High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders Vernes, Sonja C.
2007
81 6 p. 1232-1250
19 p.
artikel
11 Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain Spiteri, Elizabeth
2007
81 6 p. 1144-1157
14 p.
artikel
12 Multifactor Dimensionality Reduction–Phenomics: A Novel Method to Capture Genetic Heterogeneity with Use of Phenotypic Variables Mei, H.
2007
81 6 p. 1251-1261
11 p.
artikel
13 Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases Zhernakova, Alexandra
2007
81 6 p. 1284-1288
5 p.
artikel
14 Pathway-Based Approaches for Analysis of Genomewide Association Studies Wang, Kai
2007
81 6 p. 1278-1283
6 p.
artikel
15 Propionic and Methylmalonic Acidemia: Antisense Therapeutics for Intronic Variations Causing Aberrantly Spliced Messenger RNA Rincón, A.
2007
81 6 p. 1262-1270
9 p.
artikel
16 RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies Antoniou, Antonis C.
2007
81 6 p. 1186-1200
15 p.
artikel
17 So Many Correlated Tests, So Little Time! Rapid Adjustment of P Values for Multiple Correlated Tests Conneely, Karen N.
2007
81 6 p. 1158-1168
11 p.
artikel
18 The Structure of Common Genetic Variation in United States Populations Guthery, Stephen L.
2007
81 6 p. 1221-1231
11 p.
artikel
19 This Month in the Journal Williamson, Robin E.
2007
81 6 p. i-ii
nvt p.
artikel
20 Type 2 NF1 Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination Steinmann, Katharina
2007
81 6 p. 1201-1220
20 p.
artikel
                             20 gevonden resultaten
 
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