PAX1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in Situ hybridization (ISH and FISH)-Reference-Cited by-同舟云学术

PAX1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in Situ hybridization (ISH and FISH)

Published:1992-11 Issue:3 Volume:14 Page:740-744
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Schnittger Susanne,Gopal Rao V.V.N.,Deutsch Urban,Gruss Peter,Balling Rudi,Hansmann Ingo

Publisher

Elsevier BV

Subject

Genetics

Reference45 articles.

1. Hox and HOM, homologous gene clusters in insects and vertebrates;Akam;Cell,1989

2. Alagille syndrome and deletion of 20p;Anad;J. Med. Genet.,1990

3. undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax-1;Balling;Cell,1988

4. Allocation of a transgenic c-myc integration site to mouse chromosome 8B3-C1;Beermann;Cytogenet. Cell Genet.,1989

5. Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila;Bopp;Cell,1986

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