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deletion

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deletion

deletion Sentence Examples

  • accidental deletion of large numbers of records.

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  • According to a 1999 study, 6 percent of children with DiGeorge syndrome inherited the deletion from a parent, while 94 percent had a new deletion.

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  • The mutations in this gene are point mutations because they involve a change (either deletion, substitution, or insertion) at one specific component of a gene.

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  • Children born with this chromosomal deletion have a characteristic mewing cat-like cry as infants that is thought to be caused by abnormal development of the larynx (organ in the throat responsible for voice production).

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  • Cri du chat syndrome is also called 5p minus syndrome or chromosome 5p deletion syndrome because it is caused by a deletion, or removal, of genetic material from chromosome 5.

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  • Although most children with DiGeorge syndrome do not inherit the chromosome deletion from their parents, they have a 50 percent chance of passing the deletion on to their own children.

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  • If a child has PWS due to a sporadic deletion in the paternal chromosome 15, the chance the parents could have another child with PWS is less than 1 percent.

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  • Although methylation testing can accurately diagnose PWS, it cannot determine if the PWS is caused by a deletion, maternal uniparental disomy, or a mutation that disrupts imprinting.

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  • coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host.

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  • May 1963 Deletion of chrome trim previously fitted within instrument cowl (barely visible in most contemporary photos ).

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  • deletion of chromosome 22 called 22q11.

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  • deletion of the genes.

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  • deletion of the clause regarding an upper size limit.

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  • deletion of paragraph 153.

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  • deletion of the long arm of chromosome 13.

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  • You will be asked to confirm deletion - be brave - select the YES button!

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  • You may request deletion of your Holistic Listings member details by sending an email to Holistic Listings.

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  • At diagnosis, the incidence of p16 homozygous and hemizygous deletion in this group was 32% and 20% respectively.

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  • deletion mutants for this gene have identified three classes of upstream elements that are essential for cAMP regulation.

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  • The large fragment deletion mutations were located in a hot spot for deletion mutations were located in a hot spot for deletion that has been reported.

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  • deletion mapping using a larger group of patients is one approach to isolate single genes within critical intervals.

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  • On 27 October 2003 he was found guilty of that charge, under deletion of the words " and permanent disfigurement " .

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  • exon deletion in the RB1 gene were detected from genomic DNA.

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  • Typically a mutation in one of these genes causes exon skipping with the deletion of exon 6 from the corresponding mRNA.

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  • DNA transformation analysis of promoter deletion mutants for this gene have identified three classes of upstream elements that are essential for cAMP regulation.

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  • schwa deletion.

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  • schwa deletion pattern is not ingrained in the model itself.

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  • This somewhat tedious process guards against the accidental deletion of large numbers of records.

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  • Similarly p lines rs of deletion intersecting in p 2 points yield corresponding determinants of orders p and n-p respectively.

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  • r) does not involve any official tinge, which would justify the deletion of Kai Teµ66Eos 6 65€X00s, uou in that verse, and of r)µwv in vv.

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  • An attempt has been made to publish separately the Index Librorum Expurgandorum or Expur- gatorius, a catalogue of the works which may be read after the deletion or amending of specified passages; but this was soon abandoned.

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  • In other words, the work does not explain why there is schwa deletion.

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  • In other words, the schwa deletion pattern is not ingrained in the model itself.

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  • Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch.

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  • This will free room on your recorder without necessitating the deletion of past recordings.

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  • WS is thought to be caused by a deletion of genetic information on chromosome 7.

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  • As of 2004, it was possible to test a child's genes for the deletion that causes WS.

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  • A test technique known as fluorescent in situ hybridization (FISH) may be used to detect this deletion.

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  • Hemoglobin H disease results from the deletion of three of the four alpha globin genes.

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  • This syndrome can be caused by a deletion of a significant amount of chromosome 16, affecting the alpha globin genes.

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  • Alpha thalassemia major results from the deletion of all four alpha globin genes, such that there are no functioning alpha globin genes.

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  • Immunoglobulin heavy chain deletion, a form of agammaglobulinemia, is a genetic disorder in which part of the antibody molecule is absent.

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  • The deletion that causes cri du chat syndrome occurs on the short or p arm of chromosome 5.

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  • In 90 percent of children with cri du chat syndrome, the deletion is sporadic.

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  • If a child has cri du chat due to a sporadic deletion, the chance the parents could have another child with cri du chat is 1 percent.

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  • In approximately 10 percent of children with cri du chat, there is a hereditary chromosomal rearrangement that causes the deletion.

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  • In some cases the deletion of material from chromosome 5 can be easily seen.

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  • DiGeorge syndrome is a genetic syndrome most frequently associated with a chromosomal deletion (22q11.2).

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  • The type of defect that is involved is called deletion.

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  • A deletion occurs when the genetic material in the chromosomes does not recombine properly during the formation of sperm or egg cells.

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  • The deletion means that several genes from chromosome 22 are missing in children with DiGeorge syndrome.

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  • If the deletion is on the chromosome 15 inherited from one's mother, a different syndrome develops.

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  • This deletion occurs in a specific region on the q arm of chromosome 15.

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  • In 99 percent of the cases of PWS, the deletion is sporadic.

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  • In fewer than 1 percent of the cases of PWS there is a chromosomal rearrangement in the family that causes the deletion.

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  • Chromosome analysis can determine if the PWS is the result of a deletion in the q arm of chromosome 15.

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  • In some cases the deletion of material from chromosome 15 can be easily seen.

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  • All inquiries containing personally identifiable information are subject to deletion.

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  • However, if you lose a downloaded file due to computer errors or accidental deletion, you will have to buy a new copy of the song.

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  • The amount of time between requesting the deletion and having your information physically removed can be up to 14 days.

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  • hemizygous deletion in this group was 32% and 20% respectively.

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  • DiGeorge syndrome is a rare congenital disease that affects an infant's immune system and that is due to a large deletion from chromosome 22.

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