Joey E. Cheong-Lai

Windsor, NIR, United Kingdom

Last Updated: 09/26/2026

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Found 17 publications

Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder.

Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder.

Journal: Human molecular genetics

Published: July 19, 2021

Is adermatoglyphia an additional feature of Kindler Syndrome?

Is adermatoglyphia an additional feature of Kindler Syndrome?

Journal: Anais brasileiros de dermatologia

Published: September 17, 2015

Interstitial granulomatous drug reaction induced by quetiapine.

Interstitial granulomatous drug reaction induced by quetiapine.

Journal: Clinical and experimental dermatology

Published: November 14, 2014

Somatic forward (nonrevertant) mosaicism in recessive dystrophic epidermolysis bullosa.

Somatic forward (nonrevertant) mosaicism in recessive dystrophic epidermolysis bullosa.

Journal: JAMA dermatology

Published: July 04, 2014

Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation.

Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation.

Journal: Nature medicine

Published: November 14, 2013

Chemical atopy.

Chemical atopy.

Journal: Contact dermatitis

Published: March 21, 2013

Revertant mosaicism in the skin.

Revertant mosaicism in the skin.

Journal: Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia

Published: February 15, 2013

Pathogenesis-based therapies in ichthyoses.

Pathogenesis-based therapies in ichthyoses.

Journal: Dermatologic therapy

Published: February 07, 2013

Sporadic Kindler syndrome with a novel mutation.

Sporadic Kindler syndrome with a novel mutation.

Journal: Anais brasileiros de dermatologia

Published: October 03, 2012

Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome.

Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome.

Journal: The British journal of dermatology

Published: July 28, 2012

MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans.

MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans.

Journal: Clinical and experimental dermatology

Published: July 24, 2012

Case of Kindler syndrome resulting from mutation in the FERMT1 gene.

Case of Kindler syndrome resulting from mutation in the FERMT1 gene.

Journal: The Journal of dermatology

Published: June 08, 2012

Showing 1-12 of 17

Last Updated: 09/26/2026