A syndrome combining severe hypotrichosis and macular dystrophy: absence of mutations in TIMP genes
- 1 October 2000
- journal article
- research article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 143 (4) , 902-904
- https://doi.org/10.1046/j.1365-2133.2000.03803.x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritanceOphthalmic Genetics, 1995
- Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyNature Genetics, 1994
- Hereditary hypotrichosis of the scalpAmerican Journal of Medical Genetics, 1991
- Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: A new autosomal dominant syndromeAmerican Journal of Medical Genetics, 1990
- Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition.Journal of Medical Genetics, 1989
- Retinal Pigment Epithelium Function in Alopecia AreataJournal of Investigative Dermatology, 1986
- Congenital universal alopecia, mental deficiency, and microcephaly in two sibsJournal of Medical Genetics, 1982
- A previously undescribed condition: tricho-odonto-onycho-dermal syndrome. A review of the tricho-odonto-onychial subgroup of ectodermal dysplasiasBritish Journal of Dermatology, 1981