Jinghua Yin
Beijing, China
Last Updated: 09/26/2026
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Found 8 publications
Clinical and molecular epidemiological study of xeroderma pigmentosum in China: A case series of 19 patients.
Journal: The Journal of dermatology
Published: March 23, 2016
Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis.
Journal: Gene
Published: December 18, 2014
Compound heterozygous PLEC mutations in a patient of consanguineous parentage with epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia.
Journal: International journal of dermatology
Published: September 12, 2014
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome.
Journal: Human molecular genetics
Published: August 30, 2014
New and recurrent SERPINB7 mutations in seven Chinese patients with Nagashima-type palmoplantar keratosis.
Journal: The Journal of investigative dermatology
Published: February 12, 2014
Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia type.
Journal: The Journal of investigative dermatology
Published: July 23, 2013
Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia.
Journal: American journal of human genetics
Published: July 08, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026