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~0.5 Mb chromosomal duplications mediated by nonallelic homologous recombination between intron 22 homologous region 1 ( int22h1 ) and 2(passive) is caused byInt22h1 / int22h2-mediated Xq28 duplication syndrome
loss- and gain - of - function mutations in MeCP2(passive) are caused byRett syndrome and MeCP2 duplication syndrome
heterozygous missense mutations in the SAM domain of p63(passive) is caused byHay?Wells syndrome
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
genomic stabilitycontributingto 17p13.3 duplication syndrome
genomic stabilitypotentially contributingto 17p13.3 duplication syndrome
duplication of DNA on the Xq28 region of the chromosome(passive) is usually caused byThe MECP2 Duplication Syndrome
Williams - Beuren syndrome ( WBS ) and duplicationscauseWBS duplication syndrome
the loss - of - function mutationscauseRett syndrome and duplication
a second copy of the gene(passive) is caused byMECP2 Duplication Syndrome
a duplication of the Xq28 region of the X chromosome ( 5(passive) is typically caused byMeCP2 duplication syndrome
a genomic duplication(passive) is caused byMECP2 duplication syndrome
having an extra copy ( or two ) of the MECP2 gene and sometimes other genes in the vicinity(passive) is caused byThe duplication syndrome
an increase in this proteincausesMECP2 Duplication Syndrome
a genetic change in which there is an(passive) is caused byMECP2 duplication syndrome
The genetic abnormalitycausesMECP2 duplication syndrome
by mutations in the MECP2 gene(passive) are causedDuplication Syndrome
in 2005(passive) was discoveredMECP2 Duplication Syndrome
in 2005(passive) was discoveredMECP2 Duplication Syndrome MECP2 Duplication Syndrome
in 2005(passive) was discoveredDuplication Syndrome MECP2 Duplication Syndrome
duplication of DNA on the Xq28 region of the chromosome(passive) is usually caused byDuplication Syndrome
duplication of DNA on the Xq28 region of the chromosome(passive) is usually caused by Duplication Syndrome
duplications in a chromosomal region that typically results in cognitive impairments(passive) is caused by15q Duplication , a syndrome
the duplication of genetic material on a specific region on the X chromosome(passive) is caused byduplication syndrome
a duplication of genetic material on the long ( q ) arm of chromosome 7(passive) is caused by7q11.23 duplication syndrome
the straightforward genetic mutationcausingMECP2 Duplication Syndrome
the duplication of genetic material on a specific region on the X chromosome ( Xq28(passive) is caused byduplication syndrome
the remaining functions of the mutant allelescan causeMECP2 duplication syndrome
the same gene as Rett Syndrome(passive) is caused byDuplication Syndrome
actin - extracellular - matrix linker protein UNC-112causesKindler syndrome
Loss of kindlin-1 , a human homolog of the C. elegans actin - extracellular matrix linker protein UNC-112causesKindler syndrome
Postnatalcauses Malformations syndrome
a genetic change in which there is an(passive) is caused byduplication syndrome
that factorcausingduplication syndrome
in 2005(passive) was discoveredDuplication Syndrome
the difference between each disease ... if they overlapcausingoverlap syndrome
if they overlapcausingoverlap syndrome
other drugscauseOVERLAP SYNDROME
the straightforward genetic mutationcausingDuplication Syndrome
any drugcausingOVERLAP SYNDROME
the developmental problems(passive) caused bythe developmental problems
from a duplication that is present on the Y chromosome , or one of the autosomes ( chromosomesresultsfrom a duplication that is present on the Y chromosome , or one of the autosomes ( chromosomes
the neurotoxicity(passive) caused bythe neurotoxicity
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
a variety of neurological and behavioral problems as well as other abnormalitiescan causea variety of neurological and behavioral problems as well as other abnormalities
alsocontributesalso
cancercan causecancer
in reduced pain responsesmay resultin reduced pain responses
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
severe nerve pain stemming from my lower back down both legscausedsevere nerve pain stemming from my lower back down both legs
in a twin gestationresultedin a twin gestation
extreme fatigue and other health problemsmay causeextreme fatigue and other health problems
an increased risk for these 2 types of cancers , of prostate cancer in mencausesan increased risk for these 2 types of cancers , of prostate cancer in men
from a homozygous nonsense mutationresultingfrom a homozygous nonsense mutation
severe cicatricial ectropioncausingsevere cicatricial ectropion
in a loss of smell ( anosmiaresultsin a loss of smell ( anosmia
underdevelopment of the hypothalamus which leads to a decrease in testosterone productioncausesunderdevelopment of the hypothalamus which leads to a decrease in testosterone production
a variety of symptoms , including lower back pain , pain in the legs , buttocks , pelvis , and groincausesa variety of symptoms , including lower back pain , pain in the legs , buttocks , pelvis , and groin
Lifelong hyposmia(passive) could be caused byLifelong hyposmia
the portal venous system(passive) caused bythe portal venous system
in subfertilitymay resultin subfertility
a type of heart disease that weakens and enlarges the muscles of the heartcausesa type of heart disease that weakens and enlarges the muscles of the heart
from repair of DSBsresultingfrom repair of DSBs