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- 8p23.1_duplication_syndrome abstract "8p23.1 duplication syndrome is a rare genetic disorder caused by a duplication of a region from human chromosome 8. This duplication syndrome has an estimated prevalence of 1 in 64,000 births and is the reciprocal of the 8p23.1 deletion syndrome. The 8p23.1 duplication is associated with a variable phenotype including one or more of speech delay, developmental delay, mild dysmorphism, with prominent forehead and arched eyebrows, and congenital heart disease (CHD).".
- 8p23.1_duplication_syndrome wikiPageExternalLink 85.
- 8p23.1_duplication_syndrome wikiPageID "28202023".
- 8p23.1_duplication_syndrome wikiPageRevisionID "604687085".
- 8p23.1_duplication_syndrome hasPhotoCollection 8p23.1_duplication_syndrome.
- 8p23.1_duplication_syndrome name "8".
- 8p23.1_duplication_syndrome subject Category:Genetic_disorders_with_no_OMIM.
- 8p23.1_duplication_syndrome subject Category:Mutation.
- 8p23.1_duplication_syndrome subject Category:Rare_diseases.
- 8p23.1_duplication_syndrome type Disease.
- 8p23.1_duplication_syndrome type Situation.
- 8p23.1_duplication_syndrome comment "8p23.1 duplication syndrome is a rare genetic disorder caused by a duplication of a region from human chromosome 8. This duplication syndrome has an estimated prevalence of 1 in 64,000 births and is the reciprocal of the 8p23.1 deletion syndrome. The 8p23.1 duplication is associated with a variable phenotype including one or more of speech delay, developmental delay, mild dysmorphism, with prominent forehead and arched eyebrows, and congenital heart disease (CHD).".
- 8p23.1_duplication_syndrome label "8p23.1 duplication syndrome".
- 8p23.1_duplication_syndrome sameAs m.0cn__nt.
- 8p23.1_duplication_syndrome sameAs Q4645274.
- 8p23.1_duplication_syndrome sameAs Q4645274.
- 8p23.1_duplication_syndrome wasDerivedFrom 8p23.1_duplication_syndrome?oldid=604687085.
- 8p23.1_duplication_syndrome isPrimaryTopicOf 8p23.1_duplication_syndrome.
- 8p23.1_duplication_syndrome name "8p23.1 duplication syndrome".