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Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly t...

Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly t...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_16249677

Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5

About this item

Full title

Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5

Publisher

Boston: Massachusetts Medical Society

Journal title

The New England journal of medicine, 1992-04, Vol.326 (14), p.905-909

Language

English

Formats

Publication information

Publisher

Boston: Massachusetts Medical Society

More information

Scope and Contents

Contents

THE Marfan syndrome is a common genetic disorder of connective tissue, with characteristic manifestations in the musculoskeletal, cardiovascular, and ocular systems.
1
Recently, two independent studies
2
,
3
linked the syndrome to a fibrillin gene localized on chromosome 15.
2
This finding agreed with those of previous immun...

Alternative Titles

Full title

Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_16249677

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_16249677

Other Identifiers

ISSN

0028-4793

E-ISSN

1533-4406

DOI

10.1056/NEJM199204023261401

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