(Q28118961)

English

Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism

scientific journal article

Statements

Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism (English)
1 reference
Mireille Castanet
1 reference
Maura Agostini
1 reference
Erik Schoenmakers
1 reference
Catherine Mitchell
1 reference
Stephanie Demuth
1 reference
F. Lucy Raymond
1 reference
John Schwabe
1 reference
Mark Gurnell
1 reference
V. Krishna Chatterjee
1 reference
1 August 2010
1 reference
95
1 reference
8
1 reference
4031–4036
1 reference

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit