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Qaagi - Book of Why

Causes

Effects

the duplication of genetic material on a specific region on the X chromosome that includes a gene named MECP2(passive) is caused byMECP2 duplication syndrome

Williams - Beuren syndrome ( WBS ) and duplicationscauseWBS duplication syndrome

too muchleadsto the duplication syndrome

in 2005(passive) was discoveredDuplication Syndrome

gene duplicationscauseMECP2 Duplication syndrome

problems with the same gene as Rett Syndrome(passive) is caused bySyndrome MECP2 Duplication Syndrome

a duplication of genetic material on the long ( q ) arm of chromosome 7.[1][2][3(passive) is caused by7q11.23 duplication syndrome

various duplications chromosome 15q(passive) caused byDuplication 15q syndrome

interstitial and isodicentric duplications of 15q11.2-q13.1(passive) caused byDuplication 15q syndrome ,

having an extra copy ( or two ) of the MECP2 gene and sometimes other genes in the vicinity(passive) is caused byThe duplication syndrome

The genetic abnormalitycausesMECP2 duplication syndrome

duplicated informationcauses7q11.23 duplication syndrome

a change in DNA in which there is an extra copy of the gene(passive) is caused byMECP2 duplication syndrome

a genetic change in which there is an extra copy of theMECP2 gene in each cell(passive) is caused byMECP2 duplication syndrome

duplication or triplication of(passive) caused byMECP2 duplication syndrome

an extra copy of some of the genetic material on the X chromosome which causes problems with learning and memory , motor control of the body , seizures , and recurrent infections(passive) is caused byDuplication Syndrome

mutations in the MECP2 gene(passive) caused byMECP2 duplication syndrome

a genomic duplication that spans the methyl - CpG - binding protein 2 ( MECP2 ) gene and leads to a progressive X - linked disorder of intellectual disability , autism , spasticity , and epilepsy ( Ramocki et al .(passive) is caused byMECP2 duplication syndrome

usually(passive) is ... causedDuplication Syndrome

overexpression of MECP2(passive) caused byMECP2 duplication syndrome

a 1.5-Mb duplication in the same location as the deletion in people with Williams syndrome(passive) is caused byThe 7q11.23 duplication syndrome

duplication of DNA on the Xq28 region of the chromosome(passive) is usually caused byThe MECP2 Duplication Syndrome

the straightforward genetic mutationcausingMECP2 Duplication Syndrome

The Baylor College of Medicine lab at Texas Children 's Hospital in HoustondiscoveredMECP2 Duplication syndrome

SFARI | Characterizing 22q11.2 abnormalities Duplication of a small region on chromosome 22resultingin 22q11.2 duplication syndrome

duplication of the MeCP2 gene(passive) is caused byMeCP2 duplication syndrome

A team of scientists at Baylor College of Medicine , led by Dr. Huda ZoghbidiscoveredMECP2 Duplication Syndrome

genomic stabilitycontributingto 17p13.3 duplication syndrome

Dr. ZoghbidiscoveredMECP2 Duplication Syndrome

artificially(passive) has been ... createdDuplication syndrome

the remaining functions of the mutant allelescan causeMECP2 duplication syndrome

severe cognitive and physical disabitiescausessevere cognitive and physical disabities

oftenresultsoften

immune dysfunctionalso causesimmune dysfunction

physical and mental impairmentscausesphysical and mental impairments

in aortic dilation , dissection , or rupturecan resultin aortic dilation , dissection , or rupture

a variety of neurological and behavioral problems as well as other abnormalitiescan causea variety of neurological and behavioral problems as well as other abnormalities

a very severe disability and makes it unlikely that he will become a fathercausesa very severe disability and makes it unlikely that he will become a father

and some of the similarities and differences between MECP2 Duplication Syndromewas discoveredand some of the similarities and differences between MECP2 Duplication Syndrome

from a duplication that is present on the Y chromosome , or one of the autosomes ( chromosomes 1 - 22resultsfrom a duplication that is present on the Y chromosome , or one of the autosomes ( chromosomes 1 - 22

the neurotoxicity(passive) caused bythe neurotoxicity

in reduced pain responsesmay resultin reduced pain responses

elegant and natural facets of geometry that have proven to be of central importancehas discoveredelegant and natural facets of geometry that have proven to be of central importance

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