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Qaagi - Book of Why

Causes

Effects

by multiple genes(passive) influenced byMode of Inheritance Polygenic

by an unknown number of genes(passive) to be caused byMendelian inheritance pattern

therefore(passive) is ... composedOttavia 's inheritance

mutation in the XDH gene on chromosome 2p in some cases(passive) caused byAutosomal recessive inheritance

mutation in the survival motor neuron gene ( SMN1 ) on 5q(passive) caused byAutosomal recessive inheritance

mutation in the histidinase gene ( HIS ) on chromosome 12q(passive) caused byautosomal recessive inheritance

mutation in the extracellular matrix protein 1(passive) caused byAutosomal recessive inheritance

mutations in either of two genes(passive) caused byautosomal recessive inheritance

a single mutant gene(passive) caused byautosomal recessive inheritance

mutation in the diastrophic dysplasia sulfate transporter gene ( DTDST ) on chromosome 5q(passive) caused byautosomal recessive inheritance

mutation in the aspartoacyclase(passive) caused byAutosomal recessive inheritance

by mutation in the uridine(passive) caused byautosomal recessive inheritance

mutation in the Pendred syndrome gene ( PDS ) on 7q(passive) caused byautosomal recessive inheritance

mutation in the fatty aldehyde dehydrogenase gene ( FALDH ) on chromosome 17p(passive) caused byautosomal recessive inheritance

by mutation in the fatty aldehyde dehydrogenase gene ( FALDH(passive) caused byautosomal recessive inheritance

mutation in the gene(passive) caused byAutosomal recessive inheritance

t complex responder genecausesnon - mendelian inheritance

complex responder genecausesnon - mendelian inheritance

mutation in the gene involved in cytochrome(passive) caused byautosomal recessive inheritance ,

mutation in the sodium iodide symporter gene ( SLC5A5 ) on 19p(passive) caused byautosomal recessive inheritance

congenital defect in the formation of cartilage collagen(passive) caused byautosomal recessive inheritance

by Carl Correns(passive) discovered bynon - Mendelian inheritance

A protein kinase encoded by the t complex responder genecausesnon - mendelian inheritance

the effect of damaging mutations and how genetic backgroundinfluencestrait inheritance

open - ended stories(passive) prompted byextragenetic inheritance

Carl Correns in 1908(passive) discovered bynon - Mendelian inheritance

how multiple allelesinfluenceinheritance of a trait

how genetic backgroundinfluencestrait inheritance

genetic backgroundinfluencestrait inheritance

how multipleinfluenceinheritance of a trait

by multiple genes at different loci and environment(passive) are influenced bypolygenic inheritance

often(passive) is ... influencedallele inheritance

the environmentcan influenceinheritance of phenotypic

traitsinfluencesthe inheritance of alleles

by gene alterations in BOTH copies of a particular gene pair(passive) are caused byrecessive inheritance

Natural selection ... traitsinfluencesthe inheritance of alleles

proteinsinfluencesthe inheritance of alleles

Natural selection ... proteinsinfluencesthe inheritance of alleles

this receptorcould causeepigenetic inheritance

in humans(passive) was discoveredEpigenetic inheritance

only when an individual inherits two gene mutations for the particular diseaseresultsonly when an individual inherits two gene mutations for the particular disease

to evolutioncontributesto evolution

to the propagation of the observed phenotypic variationcontributesto the propagation of the observed phenotypic variation

the result.[1could ... influencethe result.[1

to treatments for age - related diseasescould leadto treatments for age - related diseases

the resultcould ... influencethe result

likelycontributeslikely

stillcan ... leadstill

to a heteroplasmic stateleadingto a heteroplasmic state

to duplication of inherited membersmay leadto duplication of inherited members

to a more severe phenotype than the dominant formleadingto a more severe phenotype than the dominant form

Not all disorders(passive) are caused byNot all disorders

to premature deathleadsto premature death

Cystic fibrosis(passive) is caused byCystic fibrosis

confusion between own and inherited propertiescausesconfusion between own and inherited properties

to confliction of informationmay leadto confliction of information

osteogenesis imperfectacausesosteogenesis imperfecta

phenotypic variations or disease severity(passive) caused byphenotypic variations or disease severity

cancers(passive) are caused bycancers

from mutationsresultingfrom mutations

they are generally considered(passive) to be caused bythey are generally considered

Most ONTDs(passive) are caused byMost ONTDs

most likelycontributesmost likely

These conditionscan contributeThese conditions

phenotypes(passive) caused byphenotypes

complications(passive) caused bycomplications

to constant allele frequencies across generationsshould leadto constant allele frequencies across generations

to continuous variationcan contributeto continuous variation

family riftcausesfamily rift

metabolic phenotype through Let-7ccan causemetabolic phenotype through Let-7c

from exposure to endometriosis in uteroresultingfrom exposure to endometriosis in utero

to code reuseleadingto code reuse

others ' behaviormay influenceothers ' behavior

to a more natural expression of many problemsleadsto a more natural expression of many problems

an individual entity?s reproductive successinfluencingan individual entity?s reproductive success

Another(passive) would be caused byAnother

to the discovery of DNAleadingto the discovery of DNA

to continuous variation using two examplescan contributeto continuous variation using two examples

on the other handresultson the other hand

to headache |leadsto headache |

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