(Q41637017)

English

Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome

scientific article published on March 1, 1992

Ataxia-telangiectasia: Linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome

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scholarly article

1 reference

Europe PubMed Central

5 October 2017

Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome (English)

1 reference

Europe PubMed Central

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8 October 2022

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12

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M Lathrop

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5 October 2017

6

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C. Julier

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8 October 2022

author name string

Y. Ziv

1

1 reference

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8 October 2022

M. Frydman

2

1 reference

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8 October 2022

E. Lange

3

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8 October 2022

N. Zelnik

4

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8 October 2022

G. Rotman

5

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8 October 2022

N. G. Jaspers

7

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8 October 2022

Y. Dagan

8

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8 October 2022

D. Abeliovicz

9

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8 October 2022

H. Dar

10

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8 October 2022

Z. Borochowitz

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8 October 2022

R. A. Gatti

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8 October 2022

Y. Shiloh

14

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8 October 2022

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8 October 2022

publication date

1 March 1992

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5 October 2017

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5 October 2017

88

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619-626

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5 October 2017

6

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https://scigraph.springernature.com/pub.10.1007/bf02265285

0 references

Hereditary congenital spinocerebellar ataxia accompanied by congenital cataract and oligophrenia; a genetic and clinical investigation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro phenotype of ataxia-telangiectasia (AT) fibroblast strains: clues to the nature of the "AT DNA lesion" and the molecular defect in AT

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new chromosomal instability disorder confirmed by complementation studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo and in vitro chromosomal damage induced by LSD-25.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant of ataxia-telangiectasia with low-level radiosensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant forms of ataxia telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new chromosome instability disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage map of the human genome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLP

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further delineation of the Nijmegen breakage syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Marinesco-Sjogren syndrome. 1st anatomo-clinical study]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and mapping of a polymorphic DNA sequence MCT128.1 on chromosome 11 [D11S285]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mortality and cancer incidence in 263 patients with ataxia-telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal response of ataxia-telangiectasia cells to agents that break the deoxyribose moiety of DNA via a targeted free radical mechanism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia-telangiectasia: a variant with altered in vitro phenotype of fibroblast cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence and gene frequency of ataxia-telangiectasia in the United States

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia-without-telangiectasia. Progressive multisystem degeneration with IgE deficiency and chromosomal instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome instability syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An algorithm for automatic genotype elimination

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A detailed genetic map of the long arm of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and cytologic analysis of DNA amplification in retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human T-cell receptor CD3-gamma (CD3G)/MspI DNA polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, phi 2.22

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphism analysis and assignment of the metalloproteinases stromelysin and collagenase to the long arm of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia-telangiectasia: an inherited disorder of ionizing-radiation sensitivity in man. Progress in the elucidation of the underlying biochemical defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular hypersensitivity to neocarzinostatin in ataxia-telangiectasia skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02265285

1 reference

Europe PubMed Central

5 October 2017

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0 references

1 reference

Europe PubMed Central

5 October 2017

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