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problems with a gene located on chromosome 15 called UBE3A genes(passive) often caused byAngelman Syndrome 's
by neuromuscular incoordination(passive) caused bysyndrome - dysphagia
either the deletion of , or a mutation on , the UBE3A gene on chromosome 15(passive) is generally caused byAngelman Syndrome
a deletion or mutation in the UBE3A gene on chromosome 15(passive) is caused byAngelman syndrome
a disruption in the function of the UBE3A gene on the maternal chromosome 15(passive) is caused byAngelman syndrome
problems with a gene located on chromosome 15 called UBE3A genes(passive) 's often caused byAngelman Syndrome
a deletion of genetic material at the end of the long ( q ) arm of chromosome 11(passive) is caused byJacobsen syndrome
the mutation and deletion of maternal UBE3A genecan causeAngelman syndrome
a disruption of the expression or function of the UBE3A gene located on the maternal chromosome 15 ( q11q13(passive) is caused byAngelman syndrome
deletion of or abnormal expression of the UBE3A gene that is located on the long arm ( q ) of chromosome 15 ( 15q11-q13(passive) is caused byAngelman syndrome
by mutation in or deletion of the maternal copy of the gene(passive) is caused byAngelman syndrome
More about Angelman Syndrome Deletion of the maternally inherited copy of the UBE3A genecausesAngelman syndrome
a malfunction of the gene UBE3A in the maternal chromosome # 15(passive) is caused byAngelman syndrome
by a mutation or absence of the maternal copy of the UBE3A gene(passive) caused byAngelman syndrome
by deletion of genetic material from the long arm of chromosome 11(passive) is caused byJacobsen syndrome
the loss of a gene located on chromosome 15(passive) is caused byAngelman syndrome
Other abnormalities involving the region of chromosome 15 that contains the UBE3A genecan also causeAngelman syndrome
an error in a gene located on chromosome 15 known as the ubiquitin protein ligase(passive) is caused byAngelman syndrome
UBE3A. Mutations in the UBE3A gene are knownto causeAngelman Syndrome
loss of the maternal copy of the Ube3a gene(passive) is caused byAngelman Syndrome
by loss of the maternal copy of the Ube3a gene(passive) is caused byAngelman Syndrome
the loss of the maternal copy of the UBE3A gene(passive) is caused byAngelman syndrome
a malfunction of the gene UBE3A in the maternal chromosome(passive) is caused byAngelman syndrome
by the chromosome 15 or ubiquitin protein ligase gene(passive) to be caused byAngelman syndrome
by a defect in the heart(passive) is causedEisenmenger syndrome
deletion or abnormal expression of the UBE3A gene(passive) is caused byAngelman syndrome
by deletion or inactivation of genes on the maternally inherited chromosome 15(passive) is ... caused byAngelman syndrome
the mutations in the UBE3A genecauseAngelman Syndrome
by mutations in the UBE3A gene(passive) caused byAngelman syndrome
a loss of function in the UBE3A gene on the maternal 15th chromosome(passive) is caused byAngelman syndrome
loss of expression of the UBE3A gene in the(passive) is caused byAngelman Syndrome
by a mutation in the UBE3A gene(passive) is caused byAngelman syndrome
Deletion of the same region on the maternal chromosomecausesAngelman syndrome
by the absence of the maternal copy of the UBE3A gene(passive) is caused byAngelman syndrome
due to the absence of a functional copy of the UBE3A gene , which is inherited from the mother(passive) is causedAngelman syndrome
a severe reduction of expression of the gene UBE3a in the brain(passive) is caused byAngelman Syndrome
the loss or malfunction of the maternal copy of the UBE3A gene in neurons in specific brain regions(passive) is caused byAngelman syndrome
a lack of functional UBE3A gene in the brain(passive) is caused byAngelman syndrome
a defect with the ubiquitin - protein ligase or UBE3A gene(passive) is caused byAngelman Syndrome
by the inactivation of the inherited genes called chromosome 15(passive) to be caused byAngelman syndrome
from fluid absorption in the classic TURP which is still performed in many hospitalscan resultfrom fluid absorption in the classic TURP which is still performed in many hospitals
a wide range of symptoms and physical defectscausesa wide range of symptoms and physical defects
cold hands and feetcausingcold hands and feet
development delays , severe speech impairment , intellectual disability , problems with movement and balance , and seizurescausesdevelopment delays , severe speech impairment , intellectual disability , problems with movement and balance , and seizures
from heterozygous mutations in the PTCH1 generesultsfrom heterozygous mutations in the PTCH1 gene
an increased risk of developing cancers of the skincausesan increased risk of developing cancers of the skin
severe delays or mental retardation and problems with speechcausessevere delays or mental retardation and problems with speech
to mental retardation , speech impairment and brain seizuresleadsto mental retardation , speech impairment and brain seizures
extensive deterioration in the quality of lifecausesextensive deterioration in the quality of life
to developmental delays , speech difficulties , seizures and walking or balance difficultiescan leadto developmental delays , speech difficulties , seizures and walking or balance difficulties
learning difficulties , speech problems , and seizurescauseslearning difficulties , speech problems , and seizures
severe development delayscausessevere development delays
from a loss of gene activity ( expression ) in a specific part of chromosome 15 in each cellresultsfrom a loss of gene activity ( expression ) in a specific part of chromosome 15 in each cell
a variety of physical and developmental delays in childrencausesa variety of physical and developmental delays in children
from a loss of gene activity in a specific part of chromosome 15 , the 15q11-q13 regionresultsfrom a loss of gene activity in a specific part of chromosome 15 , the 15q11-q13 region
developmental disability and seizurescausesdevelopmental disability and seizures
from a loss of gene activity ( expressionresultsfrom a loss of gene activity ( expression
chronic anemia , and anemia(passive) caused bychronic anemia , and anemia
droopy upper eyelidscausesdroopy upper eyelids
seizures , delayed milestones , balance issues , and most have no functional speechcausesseizures , delayed milestones , balance issues , and most have no functional speech
severe deficitscausessevere deficits
movement and balance disordersalso causesmovement and balance disorders
movement and balance disordersalso causesmovement and balance disorders
anemia(passive) caused byanemia
in severe learning difficultiesresultsin severe learning difficulties
severe intellectual and physical disabilitycausessevere intellectual and physical disability
seizures(passive) caused byseizures
mental retardation and impaired speechcausesmental retardation and impaired speech
severe seizures and an obsession with watercausessevere seizures and an obsession with water
developmental delay and lack of speechcausesdevelopmental delay and lack of speech
to leukemialedto leukemia
developmental delayscausesdevelopmental delays
to acute myeloid leukemialeadingto acute myeloid leukemia
usuallycausesusually
from the loss of function of a generesultfrom the loss of function of a gene
mental retardationcausesmental retardation
Pulmonary hypertension(passive) caused byPulmonary hypertension
developmental delay and neurological problemscausesdevelopmental delay and neurological problems
developmental delays , seizures , and frequent smiling and laughingcausesdevelopmental delays , seizures , and frequent smiling and laughing
from this deletionresultsfrom this deletion