Template linking and transclusion check

Checks and reports which articles that transcludes a template that are not linked from the template, and which articles that are linked from a template but do not transclude it.

(including namespace)

Results for Şablon:Kromozomal anomaliler (edit)

Mismatch between transclusions and links
Transclusion but no linkLink but no transclusion

Total: 0

Total: 38
22q11.2 delesyon sendromu (create)
49 XXXXY sendromu (create)
Burkitt's lenfoma (create)
Cat gözü sendromu (create)
Fragile X sendromu (create)
Genomik imprinting (create)
Gonadal disgenezis (create)
ICD-10 Chapter Q (create)
Karışık gonadal disgenezis (create)
Kromozom 13 (insan) (edit)
Kromozom 15 (insan) (edit)
Kromozom 17 (insan) (edit)
Kromozom 18 (insan) (edit)
Kromozom 21 (insan) (edit)
Kromozom 22 (insan) (edit)
Kromozom 4 (insan) (edit)
Kromozom 5 (insan) (edit)
Kromozom 7 (insan) (edit)
Kromozom 8 (insan) (edit)
List of ICD-9 codes 740-759: Congenital anomalies (create)
Monozomi (create)
Otozomlar (edit)
Patoloji (edit)
Philadelphia kromozomu (create)
Prader-Willi sendromu (create)
Smith-Magenis sendromu (create)
Translokasyonlar (create)
Triple X sendromu (create)
Trizomi 16 (create)
Trizomi 22 (create)
Trizomi 9 (create)
Uniparental disomi (create)
Warkany sendromu 2 (create)
Wolf-Hirschhorn sendromu (create)
XXXXX sendromu (create)
XXXX sendromu (create)
X Kromozomu (edit)
Y Kromozomu (edit)

 Links to redirects

Total: 1
Angelman Sendromu (edit) Angelman sendromu (edit)


Complete report...

Generated: Mon, 19 Nov 2018 04:08:32 UTC. Duration: 0 seconds.

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