Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family (Q33569875)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family |
scientific article |
Statements
1 reference
Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family (English)
1 reference
Jirko Kühnisch
1 reference
Sascha Vermeer
1 reference
Cor Cremers
1 reference
Hannie Kremer
1 reference
Angelien Heister
1 reference
Krysta Voesenek
1 reference
Eva Morava
1 reference
Jefte M Drijvers
1 reference
Joris H Robben
1 reference
Petra van Setten
1 reference
Amanda Branten
1 reference
Sabine Stumpp
1 reference
Alphons de Jong
1 reference
Hedi L Claahsen-van der Grinten
1 reference
Charles W O'Neill
1 reference
Michèl A Willemsen
1 reference
Dirk Lefeber
1 reference
Peter M T Deen
1 reference
Uwe Kornak
1 reference
Ron A Wevers
1 reference
13 October 2010
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference