Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism (Q48828636)

From Wikidata

Jump to navigation Jump to search

scientific article published in January 1983

edit

Language	Label	Description	Also known as
English	Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism	scientific article published in January 1983

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

title

Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

main subject

hair diseases

1 reference

based on heuristic

inferred from title

author name string

P Wieacker

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

N Horn

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

P Pearson

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

T F Wienker

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

E McKay

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

H H Ropers

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

publication date

1 January 1983

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

volume

64

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

page(s)

139-142

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

cites work

The human gene map, 20 October 1982

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a cDNA clone for human X-linked 3-phosphoglycerate kinase by use of a mixture of synthetic oligodeoxyribonucleotides as a detection probe

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes' X-linked disease: prenatal diagnosis and carrier detection

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes X-linked disease: prenatal diagnosis of hemizygous males and heterozygous females

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis with misclassification at one locus.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathology of Menkes' disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The frequency and distribution of chiasmata in man.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary defect in copper transport underlies mottled mutants in the mouse

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synaptosomal complexes and associated structures in microspread human spermatocytes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use and limitations of chiasma scoring with reference to human genetic mapping

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of crossing-over in mouse chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid sulfatase activity in cultured fibroblasts of XX males

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mapping of human chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6576980

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00327110

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

PubMed publication ID

6576980

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6576980

retrieved

15 February 2018

reference URL

http://europepmc.org/abstract/MED/6576980

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48828636&oldid=2211780585"