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Novel and recurrent FERMT1 gene mutations in Kindler syndrome. [electronic resource] by
- Techanukul, Tanasit
- Sethuraman, Gomathy
- Zlotogorski, Abraham
- Horev, Liran
- Macarov, Michal
- Trainer, Alison
- Fong, Kenneth
- Lens, Marko
- Medenica, Ljiljana
- Ramesh, Venkatesh
- McGrath, John A
- Lai-Cheong, Joey E
Producer: 20110826
In:
Acta dermato-venereologica vol. 91
Availability: No items available.
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Revertant mosaicism in recessive dystrophic epidermolysis bullosa. [electronic resource] by
- Almaani, Noor
- Nagy, Nikoletta
- Liu, Lu
- Dopping-Hepenstal, Patricia J C
- Lai-Cheong, Joey E
- Clements, Suzanne E
- Techanukul, Tanasit
- Tanaka, Akio
- Mellerio, Jemima E
- McGrath, John A
Producer: 20100702
In:
The Journal of investigative dermatology vol. 130
Availability: No items available.
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Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation. [electronic resource] by
- Lai-Cheong, Joey E
- Parsons, Maddy
- Tanaka, Akio
- Ussar, Siegfried
- South, Andrew P
- Gomathy, Sethuraman
- Mee, John B
- Barbaroux, Jean-Baptiste
- Techanukul, Tanasit
- Almaani, Noor
- Clements, Suzanne E
- Hart, Ian R
- McGrath, John A
Producer: 20091209
In:
The American journal of pathology vol. 175
Availability: No items available.
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The molecular skin pathology of familial primary localized cutaneous amyloidosis. [electronic resource] by
- Tanaka, Akio
- Lai-Cheong, Joey E
- van den Akker, Peter C
- Nagy, Nikoletta
- Millington, George
- Diercks, Gilles F H
- van Voorst Vader, Pieter C
- Clements, Suzanne E
- Almaani, Noor
- Techanukul, Tanasit
- Hide, Michihiro
- South, Andrew P
- McGrath, John A
Producer: 20110113
In:
Experimental dermatology vol. 19
Availability: No items available.
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