Found: 5
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Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.
- Published in:
- Pediatric Dermatology, 2023, v. 40, n. 6, p. 1021, doi. 10.1111/pde.15440
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- Publication type:
- Article
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy.
- Published in:
- British Journal of Dermatology, 2022, v. 187, n. 5, p. 826, doi. 10.1111/bjd.21774
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- Publication type:
- Article
Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence*.
- Published in:
- British Journal of Dermatology, 2022, v. 187, n. 3, p. 392, doi. 10.1111/bjd.21674
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- Publication type:
- Article
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti‐tumour necrosis factor‐α and interleukin‐12/23 blockade.
- Published in:
- British Journal of Dermatology, 2022, v. 186, n. 6, p. 1026, doi. 10.1111/bjd.20978
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- Article
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2879, doi. 10.1002/ajmg.a.62924
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- Publication type:
- Article