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検索結果 1 - 20 結果 / 65 検索語 '(( j l code rare near ) OR ((( j body compared _ nortes ) OR ( _ nad compared law now ))))', 処理時間: 1.45秒 結果の絞り込み
Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13–15
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways

Codon choice and potential complementarity between mRNA downstream of the initiation codon and bases 1471-1480 in 16S ribosomal RNA affects expression of glnS.
Common genetic variation in and near the melanocortin 4 receptor gene (MC4R) is associated with body mass index in American Indian adults and children

Multiplexed Targeted Resequencing Identifies Coding and Regulatory Variation Underlying Phenotypic Extremes of HDL-Cholesterol in Humans
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset
Estimating Population Cause-Specific Mortality Fractions from in-Hospital Mortality: Validation of a New Method

Diversity and Impact of Rare Variants in Genes Encoding the Platelet G Protein-Coupled Receptors
Nature and significance of the recent carbonate mound record the mound challenger code /

Variants in Hepatocyte Nuclear Factor 4α Are Modestly Associated With Type 2 Diabetes in Pima Indians
Exome Array Analysis of Early-Onset Ischemic Stroke

Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.
Evidence of two deeply divergent co-existing mitochondrial genomes in the Tuatara reveals an extremely complex genomic organization

Sexual Selection and Mixed Sex Expression: Adolescent Protandry, Phenotypic Tradeoffs and ‘Unconventional' Sex Allocation Estimates in a Protandric-Simultaneous Hermaphrodite
Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Rare Functional Variants in Genome–wide Association Identified Candidate Genes for Non-syndromic Clefts in the African Population
Allelic Variation in the Chloroplast Division Gene FtsZ2-2 Leads to Natural Variation in Chloroplast Size

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