(Q43512701)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1483703%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

title

A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysis (English)

1 reference

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20 September 2019

2

1 reference

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20 September 2019

author name string

N Groves

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1483703%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

A Hogg

series ordinal

3

1 reference

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20 September 2019

J K Cowell

series ordinal

4

1 reference

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20 September 2019

publication date

1 December 1992

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20 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1483703%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

volume

90

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20 September 2019

page(s)

440-442

1 reference

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20 September 2019

issue

4

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https://scigraph.springernature.com/pub.10.1007/bf00220474

20 September 2019

exact match

0 references

cites work

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

12 December 2020

Reverse genetics and human disease

1 reference

12 December 2020

Tumor suppressor genes

1 reference

12 December 2020

Preferential loss of maternal alleles in sporadic Wilms' tumour.

1 reference

12 December 2020

Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT

1 reference

12 December 2020

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

1 reference

12 December 2020

A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

1 reference

12 December 2020

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1 reference

12 December 2020

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.

1 reference

12 December 2020

Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus

1 reference

12 December 2020

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

12 December 2020

Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing

1 reference

12 December 2020

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.

1 reference

12 December 2020

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1 reference

12 December 2020

Structural rearrangements of the WT1 gene in Wilms' tumour cells

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00220474

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1483703%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

20 September 2019

0 references

1 reference