(Q41202226)

English

Fanconi anaemia in Italy: high prevalence of complementation group A in two geographic clusters

scientific article published on May 1996

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Statements

scholarly article

1 reference

Europe PubMed Central

28 September 2017

Fanconi anaemia in Italy: high prevalence of complementation group A in two geographic clusters (English)

1 reference

Europe PubMed Central

28 September 2017

0 references

author name string

A Savoia

1

1 reference

Europe PubMed Central

28 September 2017

A Zatterale

2

1 reference

Europe PubMed Central

28 September 2017

D Del Principe

3

1 reference

Europe PubMed Central

28 September 2017

H Joenje

4

1 reference

Europe PubMed Central

28 September 2017

publication date

1 May 1996

1 reference

Europe PubMed Central

28 September 2017

1 reference

Europe PubMed Central

28 September 2017

97

1 reference

Europe PubMed Central

28 September 2017

599-603

1 reference

Europe PubMed Central

28 September 2017

5

1 reference

Europe PubMed Central

28 September 2017

Nomenclature of human DNA repair genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Geographical structuring in the mtDNA of Italians

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and treatment of late onset Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi anemia and novel strategies for therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic history of Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of cDNAs for Fanconi's anaemia by functional complementation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Italian contribution to the study of Fanconi's anemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of the Fanconi anemia gene FACC

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Fanconi anemia polypeptide FACC is localized to the cytoplasm

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic population structure of Italy. II. Physical and cultural barriers to gene flow

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complementation groups: one or more per gene?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation and expression of the XPA gene in revertants and hybrids of a xeroderma pigmentosum cell line.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A nonsense mutation and exon skipping in the Fanconi anaemia group C gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of two complementation groups in Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi anaemia research: current status and prospects

1 reference

https://pubmed.ncbi.nlm.nih.gov/8655138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S004390050101

1 reference

Europe PubMed Central

28 September 2017

1 reference

Europe PubMed Central

28 September 2017

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