An Alu polymorphism intragenic to the neurofibromatosis type 1 gene (NF1).

Nucleic acids research ·Vol. 19 ·No. 13 ·1991-07-11 ·Pages 3764

Xu GF, Nelson L, O'Connell P, White R

Abstract

暂无摘要

Related Genes

NF1

MeSH Terms

Alleles Base Sequence Chromosomes, Human, Pair 17 DNA, Single-Stranded/genetics Gene Frequency Genetic Markers Humans Introns/genetics Molecular Sequence Data Neurofibromatosis 1/genetics Polymerase Chain Reaction Polymorphism, Genetic Repetitive Sequences, Nucleic Acid

Chemicals

DNA, Single-Stranded Genetic Markers

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Xu G F

Department of Human Genetics, University of Utah, Salt Lake City 84112.

Nelson L

O'Connell P

White R

References (3)

3 references, click to expand

The neurofibromatosis type 1 gene encodes a protein related to GAP.
Cell. 1990 Aug 10;62(3):599-608 PMID: 2116237
The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome.
Proc Natl Acad Sci U S A. 1990 Apr;87(8):2951-4 PMID: 2326257
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations.
Genomics. 1990 Aug;7(4):547-54 PMID: 2117565

Article Info

Journal

Nucleic acids research

Abbr.

Nucleic Acids Res

ISSN

0305-1048

DOI

10.1093/nar/19.13.3764

Published

1991-07-11

Pages

3764

Language

English

Region

England

NLM ID

0411011

PMCID

PMC328440

Subset

External Links

PubMed source DOI: 10.1093/nar/19.13.3764 PMC Full Text View journal details

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An Alu polymorphism intragenic to the neurofibromatosis type 1 gene (NF1).

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