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                             21 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Common Haplotype in the G-Protein–Coupled Receptor Gene GPR74 Is Associated with Leanness and Increased Lipolysis Dahlman, Ingrid
2007
80 6 p. 1115-1124
10 p.
artikel
2 Addendum 2007
80 6 p. 1194-
1 p.
artikel
3 A Generalized Combinatorial Approach for Detecting Gene-by-Gene and Gene-by-Environment Interactions with Application to Nicotine Dependence Lou, Xiang-Yang
2007
80 6 p. 1125-1137
13 p.
artikel
4 A Genomewide Admixture Map for Latino Populations Price, Alkes L.
2007
80 6 p. 1024-1036
13 p.
artikel
5 A Genomewide Admixture Mapping Panel for Hispanic/Latino Populations Mao, Xianyun
2007
80 6 p. 1171-1178
8 p.
artikel
6 A Genomewide Single-Nucleotide–Polymorphism Panel for Mexican American Admixture Mapping Tian, Chao
2007
80 6 p. 1014-1023
10 p.
artikel
7 A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor–Mediated Cell Signaling, Causes Progressive Hearing Loss Modamio-Høybjør, Silvia
2007
80 6 p. 1076-1089
14 p.
artikel
8 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 ½-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
80 6 p. 1197-1199
3 p.
artikel
9 Arthur G. Steinberg, 1912–2006 Jenkins, Trefor
2007
80 6 p. 1009-1013
5 p.
artikel
10 ASHG Board Emphasizes Communication and Involvement Boughman, Joann A.
2007
80 6 p. 1195-1196
2 p.
artikel
11 Defining the Cause of Skewed X-Chromosome Inactivation in X-Linked Mental Retardation by Use of a Mouse Model Muers, Mary R.
2007
80 6 p. 1138-1149
12 p.
artikel
12 Gene Copy-Number Variation and Associated Polymorphisms of Complement Component C4 in Human Systemic Lupus Erythematosus (SLE): Low Copy Number Is a Risk Factor for and High Copy Number Is a Protective Factor against SLE Susceptibility in European Americans Yang, Yan
2007
80 6 p. 1037-1054
18 p.
artikel
13 Homozygosity Haplotype Allows a Genomewide Search for the Autosomal Segments Shared among Patients Miyazawa, Hitoshi
2007
80 6 p. 1090-1102
13 p.
artikel
14 Intragenic Cis and Trans Modification of Genetic Susceptibility in DYT1 Torsion Dystonia Risch, Neil J.
2007
80 6 p. 1188-1193
6 p.
artikel
15 IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma Balaci, Lenuta
2007
80 6 p. 1103-1114
12 p.
artikel
16 Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6 Golzio, Christelle
2007
80 6 p. 1179-1187
9 p.
artikel
17 RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity Jenkins, Dagan
2007
80 6 p. 1162-1170
9 p.
artikel
18 Red-Green Color Vision Impairment in Duchenne Muscular Dystrophy Costa, Marcelo Fernandes
2007
80 6 p. 1064-1075
12 p.
artikel
19 This Month in the Journal Williamson, Robin E.
2007
80 6 p. i-ii
nvt p.
artikel
20 Transcriptional Control of SLC26A4 Is Involved in Pendred Syndrome and Nonsyndromic Enlargement of Vestibular Aqueduct (DFNB4) Yang, Tao
2007
80 6 p. 1055-1063
9 p.
artikel
21 Type 2 Diabetes TCF7L2 Risk Genotypes Alter Birth Weight: A Study of 24,053 Individuals Freathy, Rachel M.
2007
80 6 p. 1150-1161
12 p.
artikel
                             21 gevonden resultaten
 
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