Pages that link to "Q843863"
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The following pages link to genetic linkage (Q843863):
Displayed 31 items.
- centimorgan (Q284100) (← links)
- Category:Genetic linkage analysis (Q8482277) (← links)
- (Q10503813) (redirect page) (← links)
- (Q12107233) (redirect page) (← links)
- (Q12566721) (redirect page) (← links)
- Role of RUNX in autoimmune diseases linking rheumatoid arthritis, psoriasis and lupus (Q24805723) (← links)
- The retroviral RNA dimer linkage: different structures may reflect different roles (Q24805913) (← links)
- Linking susceptibility genes and pathogenesis mechanisms using mouse models of systemic lupus erythematosus (Q26822662) (← links)
- The genetics of major depression (Q26830784) (← links)
- Vitiligo--part 1 (Q27028001) (← links)
- Genetic mapping in human disease (Q29614943) (← links)
- Genomic approaches to coronary artery disease (Q34530017) (← links)
- Chromosomal organization at the level of gene complexes (Q34594810) (← links)
- A survey of current software for linkage analysis (Q35985471) (← links)
- Psoriasis and other complex trait dermatoses: from Loci to functional pathways (Q36043340) (← links)
- Genetics and proteomics: deciphering gene association studies in critical illness (Q36577973) (← links)
- Meta-analysis of genome-wide linkage studies of asthma and related traits (Q36667639) (← links)
- Combining transcriptional profiling and genetic linkage analysis to uncover gene networks operating in hematopoietic stem cells and their progeny (Q36805970) (← links)
- Autism: an overview of genetic aetiology (Q37392762) (← links)
- Non-syndromic autosomal recessive mental retardation in Tunisian families : exclusion of GRIK2 and TUSC3 genes (Q39249080) (← links)
- The genetic and environmental factors for keratoconus (Q41444461) (← links)
- Variation in recombination frequency and distribution across eukaryotes: patterns and processes (Q44849961) (← links)
- Linkage analysis of six Algerian families with autosomal recessive non specific mental retardation (Q46867625) (← links)
- Identification of a new genetic entity in the form of an autosomal dominant axonal Charcot-Marie-Tooth disease associated with periodic paralyses and pyramidal syndrome (Q46871815) (← links)
- Insight into the molecular genetics of myopia (Q47701145) (← links)
- Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families (Q61804774) (← links)
- Linking genes with ecological strategies in Arabidopsis thaliana (Q90610904) (← links)
- Wikidata:Database reports/Constraint violations/P111 (← links | edit)
- Wikidata:Database reports/Units of measurements (← links | edit)
- Wikidata:Database reports/Constraint violations/P7431 (← links | edit)
- Wikidata:Database reports/Constraint violations/P10283 (← links | edit)