Prenatal diagnosis for Epidermolysis bullosa: a study of 144 consecutive pregnancies at risk
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference86 articles.
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2. A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease
3. Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities
4. A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein.
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2. Recommendations on pregnancy, childbirth and aftercare in epidermolysis bullosa: a consensus‐based guideline;British Journal of Dermatology;2021-11-25
3. A retrospective analysis of diagnostic testing in a large North American cohort of patients with epidermolysis bullosa;Journal of the American Academy of Dermatology;2021-10
4. Neonatal epidermolysis bullosa: lessons to learn about genetic counseling;Journal of Dermatological Treatment;2020-11-02
5. Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa;British Journal of Dermatology;2019-08-09
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