First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe (Q69834543)

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scientific article published on 01 January 1985

Language	Label	Description	Also known as
English	First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe	scientific article published on 01 January 1985

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scholarly article

1 reference

Europe PubMed Central

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6 October 2019

First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe (English)

1 reference

Europe PubMed Central

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6 October 2019

author name string

J Boué

1

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6 October 2019

I Oberle

2

1 reference

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6 October 2019

R Heilig

3

1 reference

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6 October 2019

J L Mandel

4

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6 October 2019

A Moser

5

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6 October 2019

H Moser

6

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6 October 2019

J W Larsen

7

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6 October 2019

Y Dumez

8

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6 October 2019

A Boué

9

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6 October 2019

publication date

1 January 1985

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6 October 2019

1 reference

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6 October 2019

69

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6 October 2019

3

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6 October 2019

272-274

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6 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00293039

0 references

Adrenoleukodystrophy: impaired oxidation of very long chain fatty acids in white blood cells, cultured skin fibroblasts, and amniocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/3856557

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/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinically useful DNA probe closely linked to haemophilia A

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal Diagnosis of Sickle-Cell Anemia in the First Trimester of Pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of female carriers of adrenoleukodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytological map of the human X chromosome--evidence for non-random recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal gland

1 reference

https://pubmed.ncbi.nlm.nih.gov/3856557

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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