(Q37580477)

English

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site

scientific article published on December 1984

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site (English)

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

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author name string

P Szabo

1

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

M Purrello

2

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

M Rocchi

3

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

N Archidiacono

4

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

B Alhadeff

5

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

G Filippi

6

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

D Toniolo

7

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

G Martini

8

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

L Luzzatto

9

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Europe PubMed Central

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21 August 2017

M Siniscalco

10

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Europe PubMed Central

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21 August 2017

language of work or name

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publication date

1 December 1984

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Europe PubMed Central

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21 August 2017

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

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Europe PubMed Central

PMC publication ID

21 August 2017

81

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Europe PubMed Central

PMC publication ID

21 August 2017

24

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Europe PubMed Central

PMC publication ID

21 August 2017

7855-7859

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Linkage of color blindness to hemophilias A and B.

1 reference

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23 August 2017

Isolation and characterization of a cDNA coding for human factor IX

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Localization of a unique gene by direct hybridization in situ

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

The fragile X: a scanning electron microscope study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Molecular cloning of the gene for human anti-haemophilic factor IX.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Triplo-X constitution of mother explains apparent occurrence of two recombinants in sibship segregating at two closely X-linked loci (G6PD and deutan)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

23 August 2017

Isolation of a human anti-haemophilic factor IX cDNA clone using a unique 52-base synthetic oligonucleotide probe deduced from the amino acid sequence of bovine factor IX.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

14 September 2017

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

14 September 2017

Gene deletions in patients with haemophilia B and anti-factor IX antibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

25 June 2018

Brief report: linkage between G6PD and fragile-X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

25 June 2018

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

25 June 2018

Chromosome banding required for studies on X-linked mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

25 June 2018

Christmas disease, color-blindness and blood group Xga

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

25 June 2018

COMBINED HEMOPHILIA AND CHRISTMAS DISEASE

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

1 September 2018

HAEMOPHILIA, CHRISTMAS DISEASE AND THE XG BLOOD GROUPS. OBSERVATIONS BASED ON THE HAEMOPHILIACS OF BIRMINGHAM.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

1 September 2018

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

1 September 2018

Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392251

1 September 2018

High resolution banding and the locus of the Xq fragile site

1 reference

https://pubmed.ncbi.nlm.nih.gov/6595664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chapter 7 The Radioiodination of RNA and DNA to High Specific Activities

1 reference

https://pubmed.ncbi.nlm.nih.gov/6595664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6595664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322

1 reference

https://pubmed.ncbi.nlm.nih.gov/6595664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.81.24.7855

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1984PNAS...81.7855S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

ResearchGate publication ID

0 references

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