(Q24595193)

11

object named as

C G Mathew

0 references

Thomy de Ravel

1 reference

ORCID Public Data File 2021

author name string

A J Tipping

1

0 references

T Pearson

2

0 references

N V Morgan

3

0 references

R A Gibson

4

0 references

L P Kuyt

5

0 references

C Havenga

6

0 references

E Gluckman

7

0 references

H Joenje

8

0 references

T de Ravel

9

0 references

S Jansen

Proceedings of the National Academy of Sciences of the United States of America

10

0 references

language of work or name

English

0 references

publication date

8 May 2001

0 references

published in

0 references

volume

98

0 references

issue

10

0 references

page(s)

5734-9

0 references

cites work

Isolation of a cDNA representing the Fanconi anemia complementation group E gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

High frequency of large intragenic deletions in the Fanconi anemia group A gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

The Fanconi anaemia group G gene FANCG is identical with XRCC9

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Sequence variation in the Fanconi anemia gene FAA

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Basic local alignment search tool

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Carrier frequency of the IVS4 + 4 A-->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Positional cloning of the Fanconi anaemia group A gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Alu repeats and human disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Medical genetics in South Africa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Recombination hot spots and human disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33282

Fanconi anemia: another disease of unusually high prevalence in the Afrikaans population of South Africa

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.091402398

Fanconi's Anaemia in the Genetics of Neoplasia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.091402398

Identification ofAlu-mediated deletions in the Fanconi anemia geneFAA

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11344308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11344308