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PMID: 2883927 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Linkage of adrenoleukodystrophy to a polymorphic DNA probe.

Annals of neurology ·Vol. 21 ·No. 4 ·1987-04-00 ·Pages 349-52

Aubourg PR, Sack GH, Meyers DA, Lease JJ, Moser HW

Abstract

Linkage studies between X-linked adrenoleukodystrophy and a cloned deoxyribonucleic acid fragment (St14), which detects polymorphisms in the distal end of the long arm of the X chromosome (Xq27-28), have shown no recombination in six families. The lod score for these data (and another kindred reported earlier is 13.766 at recombination fraction (theta) = 0.0. These data permit assignment of adrenoleukodystrophy carrier status in family members at risk, supplementing the chemical measurement of very-long-chain fatty acids.

MeSH Terms
Adrenoleukodystrophy/genetics Diffuse Cerebral Sclerosis of Schilder/genetics Female Genetic Carrier Screening Genetic Linkage Humans Male Pedigree Polymorphism, Genetic Polymorphism, Restriction Fragment Length Sex Chromosome Aberrations X Chromosome
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Aubourg P R
Sack G H
Meyers D A
Lease J J
Moser H W
Article Info
Journal
Annals of neurology
Abbr.
Ann Neurol
ISSN
0364-5134
Published
1987-04-00
Pages
349-52
Language
English
Region
United States
NLM ID
7707449
Subset
IM
Grants
NIADDK NIH HHS · AM31745-01 · United States
NICHD NIH HHS · HD10981-9 · United States
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