Journal Article

Corrigenda

in Human Molecular Genetics

Volume 8, issue 5, pages 943-943
Published in print May 1999 | ISSN: 0964-6906
Published online May 1999 | e-ISSN: 1460-2083 | DOI: http://dx.doi.org/10.1093/hmg/8.5.943
Corrigenda

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Bexl, a Gene with Increased Expression in Parthenogenetic Embryos, Is a Member of a Novel Gene Family on the Mouse X Chromosome

Anna L. Brown and Graham F. Kay

Human Molecular Genetics, 8, 611–619 (1999)

In Materials and Methods, some details in the Mapping section were listed incorrectly. The sequence polymorphisms identified in the amplified products and used for mapping were as follows: Bexl, cDNA position 417 C57BL/6 (G) and Spretus (T); Bex2, cDNA position 207 C57BL/6 (A) and Spretus (G), cDNA position 233 C57BL/6 (G) and Spretus (A), cDNA position 243 C57BL/6 (T) and Spretus (G); Bex3, cDNA position 289 C57BL/6 (A) and Spretus (C), cDNA position 603 C57BL/6 (C) and Spretus (T).

Also, in the X inactivation assay section, the cDNA position of the Lab strain (A) and PGK (G) polymorphism should be 267.

Journal Article.  0 words. 

Subjects: Genetics and Genomics

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