(Q56388262)

English

Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder

No description defined

Statements

Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder (English)
0 references
A F Lewanda
0 references
M M Cohen
0 references
J Hood
0 references
S Morsey
0 references
M Walters
0 references
J L Kennedy
0 references
E W Jabs
0 references
December 1993
0 references
147
0 references
1306-8
0 references
12
0 references

Identifiers

0 references
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit