(Q36423501)

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Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

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Europe PubMed Central

PubMed publication ID

14 August 2017

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

author name string

M H Hofker

1

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

M C Wapenaar

2

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

N Goor

3

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

E Bakker

4

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

G J van Ommen

5

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

P L Pearson

6

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Europe PubMed Central

PubMed publication ID

14 August 2017

publication date

1 January 1985

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Europe PubMed Central

PubMed publication ID

14 August 2017

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Europe PubMed Central

PubMed publication ID

14 August 2017

70

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Europe PubMed Central

PubMed publication ID

14 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

148-156

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of the human immune interferon gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies for detecting and characterizing restriction fragment length polymorphisms (RFLP's)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutation rate of the gene for haemophilia, and its segregation ratios in males and females

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxygen consumption of phagocytizing cells in human leukocyte and granulocyte preparations: a comparative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How many polymorphic genes will it take to span the human genome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human thyroglobulin gene contains two 15-17 kb introns near its 3'-end

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA restriction fragment length polymorphisms and heterozygosity in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Establishment of cell lines from normal adult human blood leukocytes by exposure to Epstein-Barr virus and neutralization by human sera with Epstein-Barr virus antibody.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that the Menkes locus maps on proximal Xp.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in Duchenne muscular dystrophy by use of cloned DNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy. Frequency of sporadic cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2989153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273073

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

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