Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis (Q28277862)

From Wikidata
Jump to navigation Jump to search
scientific article
edit
Language Label Description Also known as
English
Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis
scientific article

    Statements

    Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis (English)
    0 references
    0 references
    0 references
    0 references
    0 references
    0 references
    Catherine Dodé
    0 references
    Corinne Fouveaut
    0 references
    Geert Mortier
    0 references
    Sandra Janssens
    0 references
    Jacques Mahoudeau
    0 references
    Christine Chabrolle
    0 references
    Antoine Gancel
    0 references
    Inge François
    0 references
    Michel Pugeat
    0 references
    Alfons Pineiro-Garcia
    0 references
    Arnaud Murat
    0 references
    Philippe Bouchard
    0 references
    Jacques Young
    0 references
    Marc Delpech
    0 references
    January 2007
    0 references
    28
    0 references
    97-8
    0 references
    1
    0 references

    Identifiers

    0 references
    0 references
     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit