MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression (Q39993879)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression |
scientific article |
Statements
1 reference
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression (English)
1 reference
1 reference
Vincent des Portes
1 reference
Jean-Pierre Fryns
1 reference
Hans van Bokhoven
1 reference
Suzanna Gerarda Maria Frints
1 reference
Steffen Lenzner
1 reference
Mareike Bauters
1 reference
Lars Riff Jensen
1 reference
Hilde Van Esch
1 reference
Ute Moog
1 reference
Merryn Victor Erik Macville
1 reference
Kees van Roozendaal
1 reference
Constance Theresia Rimbertha Maria Schrander-Stumpel
1 reference
Andreas Tzschach
1 reference
Peter Marynen
1 reference
Ben Hamel
1 reference
Jamel Chelly
1 reference
Chérif Beldjord
1 reference
Gillian Turner
1 reference
Claude Moraine
1 reference
Hans Hilger Ropers
1 reference
Guy Froyen
1 reference
Andreas Walter Kuss
1 reference
9 April 2008
1 reference
1 reference
16
1 reference
9
1 reference
1029-1037
1 reference
Identifiers
1 reference
1 reference