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
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
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
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