(Q45877644)

17 December 2017

title

Frequency of recent retrotransposition events in the human factor IX gene (English)

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17 December 2017

author name string

Li X

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17 December 2017

Scaringe WA

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17 December 2017

Hill KA

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17 December 2017

Roberts S

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17 December 2017

Mengos A

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17 December 2017

Careri D

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17 December 2017

Pinto MT

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17 December 2017

Kasper CK

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17 December 2017

Sommer SS

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17 December 2017

publication date

1 June 2001

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17 December 2017

published in

Human Mutation

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17 December 2017

volume

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17 December 2017

issue

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17 December 2017

page(s)

511-519

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17 December 2017

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

cites work

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Standardized nomenclature for Alu repeats

21 January 2018

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The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene

21 January 2018

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21 January 2018

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High genomic deleterious mutation rates in hominids

21 January 2018

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The Pennsylvania hemophilia program 1973-1978.

21 January 2018

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The rate of spontaneous mutation of a human gene

21 January 2018

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Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC gene

21 January 2018

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A new subfamily of recently retroposed human Alu repeats

21 January 2018

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Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.

21 January 2018

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Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy

21 January 2018

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The rate with which spontaneous mutation alters the electrophoretic mobility of polypeptides

21 January 2018

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De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome

21 January 2018

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Potential Gene Conversion and Source Genes for Recently Integrated Alu Elements

21 January 2018

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Unit-length line-1 transcripts in human teratocarcinoma cells

21 January 2018

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The factor IX gene as a model for analysis of human germline mutations: an update

21 January 2018

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Genomic amplification with transcript sequencing

21 January 2018

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A de novo Alu insertion results in neurofibromatosis type 1

21 January 2018

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Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers

21 January 2018

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Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 gene

21 January 2018

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The recent evolution of mammalian repetitive DNA elements

21 January 2018

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L1 (LINE-1) retrotransposon evolution and amplification in recent human history

21 January 2018

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7 January 2021

Parameters affecting the yield of DNA from human blood

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7 January 2021

An estimated frequency of endogenous insertional mutations in humans

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7 January 2021

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7 January 2021

Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations

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7 January 2021

Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene

1 reference

7 January 2021

Identifiers

DOI

10.1002/HUMU.1134

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17 December 2017

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17 December 2017