A new polymorphic probe on chromosome 3p: lambda LIB18-88 (D3S1093).

M Wei; F Latif; K Tory; M Yao; M L Orcutt; B Zbar; M I Lerman

doi:10.1093/nar/19.16.4575

PubMed · 1715988

A new polymorphic probe on chromosome 3p: lambda LIB18-88 (D3S1093).

M Wei·F Latif·K Tory·M Yao·M L Orcutt·B Zbar·M I Lerman

View original source ↗Export metadata ↓

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Chromosomes, Human, Pair 3 DNA Probes Deoxyribonuclease HpaII Deoxyribonucleases, Type II Site-Specific Humans Polymorphism, Genetic White People von Hippel-Lindau Disease Journal Article Research Support, U.S. Gov't, P.H.S.

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

M Wei, F Latif, K Tory, M Yao, M L Orcutt, B Zbar, M I Lerman. 1991-08-25. A new polymorphic probe on chromosome 3p: lambda LIB18-88 (D3S1093).. https://doi.org/10.1093/nar%2F19.16.4575

Cite the original work for its findings. Save a collection to share your selection of sources.

A new polymorphic probe on chromosome 3p: lambda LIB18-88 (D3S1093).

Abstract

Explore related subjects

Keep this discovery

Related citations

Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin.

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.

Two TaqI RFLPs at the GLUT2 locus in French Caucasian population.