Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy (Q24676719)

From Wikidata
Jump to navigation Jump to search
scientific article
edit
Language Label Description Also known as
English
Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy
scientific article

    Statements

    Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy (English)
    0 references
    J Kohlhase
    0 references
    L Schubert
    0 references
    M Liebers
    0 references
    A Rauch
    0 references
    K Becker
    0 references
    S N Mohammed
    0 references
    R Newbury-Ecob
    0 references
    W Reardon
    0 references
    July 2003
    0 references
    40
    0 references
    7
    0 references
    473-8
    0 references

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit