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- Mendelian_genetics_of_humans_exophenotype abstract "Mendelian genetics of humans exophenotype deals only with properties in the domain of qualitative variations and /or that quantitative properties that can be described in arbitrary categories, such as it were Mendel’s variety of low and high pea stalks. Therefore, this area classical genetics coverages of only those properties that behave according to the model monogenic inheritance, i.e. simple gene inheritance.According to the model Mendelian inheritance, if a child, at least from one of the parents gets dominant allele will have dominant phenotypic variant of observed properties. Only those who get a recessive allele from both parents exhibit the recessive phenotypes. Those who gets dominant allele from one parent and recessive than the other, will be the dominant variant features.Among the infinitely large number of potentially describable feature, very few that can be introduced in a purely Mendelian traits, because most of the phenotypic expression of the exophenotypic traits is the showpiece incomplete dominance, codominance and quantitative contributions from smaller or larger number of genes (see: Polygenic inheritance, Oligogenic inheritance).Theoretically, the recessive phenotype can skip any number of generations, remaining "dormant" in heterozygous "carriers", until they have children with someone who has one or both recessive alleles, which will transfer to his/her child. If second partnet is recessive homozygote, the chance for expression of recessive phenotype is 50%, and if, as mentioned holder, and he heterozygote, in their offspring will appear 25% of individuals with recessive phenotype.The studies of the morphological - anatomical, undoubtedly inherited properties, faces particular difficulties because of incomplete gene expressiveness or penetrance which control them, regardless of their affiliation to any of the described models of inheritance.Most of those traits that exhibit a high heritability degree was listed in hardcover McKusick's Mendelian Inheritance in Man until the 10's editions. Many of them are still included in today's OMIM's edition.Before the discovery of DNA identification, many of these features are worldwide used as the genetic markers in medicolegal practice, including the cases of disputed paternity.".
- Mendelian_genetics_of_humans_exophenotype wikiPageExternalLink intersnp.meb.uni-bonn.de.
- Mendelian_genetics_of_humans_exophenotype wikiPageExternalLink www.geneticinteractions.org.
- Mendelian_genetics_of_humans_exophenotype wikiPageExternalLink omim.
- Mendelian_genetics_of_humans_exophenotype wikiPageID "45462960".
- Mendelian_genetics_of_humans_exophenotype wikiPageLength "13635".
- Mendelian_genetics_of_humans_exophenotype wikiPageOutDegree "68".
- Mendelian_genetics_of_humans_exophenotype wikiPageRevisionID "678962313".
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Acne_vulgaris.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Allele.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Anatomy.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Aquiline_nose.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Brachydactyly.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Cartilage–hair_hypoplasia.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Category:Classical_genetics.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Category:Human_genetics.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Cenani_Lenz_syndactylism.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Cenani–Lenz_syndactylism.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Classical_genetics.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Cleft_chin.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Codominance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Cystic_fibrosis.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink DNA.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Dimple.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Dominance_(genetics).
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Earlobe.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Earwax.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Epistasis.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Expressivity_(genetics).
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Feature_(machine_learning).
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Features_(pattern_recognition).
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Freckle.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Freckles.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Friedreichs_ataxia.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Galactosemia.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Gene.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Gene_interaction.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Genetic_marker.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Gregor_Mendel.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Hair_whorl.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Heterozygote.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Heterozygous.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Hitchhikers_thumb.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Homozygote.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Huntingtons_disease.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Hypertelorism.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Hypotelorism.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Incomplete_dominance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Lactose_intolerance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Leukonychia.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Ligamentous_Laxity.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Ligamentous_laxity.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Marfan_syndrome.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Marfans_syndrome.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Mendelian_Inheritance_in_Man.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Mendelian_inheritance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Mitochondrial_neurogastrointestinal_encephalopathy_syndrome.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Morphological_(biology).
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Morphology_(biology).
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink OMIM.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Ocular_hypertelorism.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Oligogene.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Oligogenic_inheritance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Online_Mendelian_Inheritance_in_Man.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Pea.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Penetrance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Phenotype.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Phenotypic_trait.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Phenylthiocarbamide.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Photic_sneeze_reflex.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Polydactyly.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Polygenic_inheritance.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Primary_Hyperhidrosis.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Quantitative_trait_locus.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Roman_nose.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Sinus_bradycardia.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Sinus_tachycardia.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Syndactyly.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Thumb.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Trimethylaminuria.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Widows_peak.
- Mendelian_genetics_of_humans_exophenotype wikiPageWikiLink Zygosity.
- Mendelian_genetics_of_humans_exophenotype hasPhotoCollection Mendelian_genetics_of_humans_exophenotype.
- Mendelian_genetics_of_humans_exophenotype wikiPageUsesTemplate Template:Genarch.
- Mendelian_genetics_of_humans_exophenotype wikiPageUsesTemplate Template:Orphan.
- Mendelian_genetics_of_humans_exophenotype wikiPageUsesTemplate Template:Reflist.
- Mendelian_genetics_of_humans_exophenotype subject Category:Classical_genetics.
- Mendelian_genetics_of_humans_exophenotype subject Category:Human_genetics.
- Mendelian_genetics_of_humans_exophenotype hypernym u2019.
- Mendelian_genetics_of_humans_exophenotype comment "Mendelian genetics of humans exophenotype deals only with properties in the domain of qualitative variations and /or that quantitative properties that can be described in arbitrary categories, such as it were Mendel’s variety of low and high pea stalks. Therefore, this area classical genetics coverages of only those properties that behave according to the model monogenic inheritance, i.e.".
- Mendelian_genetics_of_humans_exophenotype label "Mendelian genetics of humans exophenotype".
- Mendelian_genetics_of_humans_exophenotype sameAs m.012w41r9.
- Mendelian_genetics_of_humans_exophenotype wasDerivedFrom Mendelian_genetics_of_humans_exophenotype?oldid=678962313.
- Mendelian_genetics_of_humans_exophenotype isPrimaryTopicOf Mendelian_genetics_of_humans_exophenotype.