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Bart syndrome
Gene Name 疾患和名 疾患英名 HMGCS2 3-ヒドロキシ-3-メチル
WO 2015/048577 A2 April 2015 (02.04.2015) W P O P C T
Table I. Genodermatoses with Known Gene Defects 92 Pulkkinen
Classification Meeting 2014
A Case Report of Aplasia Cutis Congenita Type VI: Bart Syndrome Florica SANDRU1,2, Catalina IORDAN3, Dana ZACIU3, Aida PETCA1,4, Mihai DUMITRASCU1,5, Adelina POPA2
7.1 Birth Defects Code List
Junctional Epidermolysis Bullosa
Guidelines for Conducting Birth Defects Surveillance
Inherited Epidermolysis Bullosa
Chromosomal Abnormalities Chromosome Mutations/Anomalies / Diseases Number 1 1
A 1A4 Antibodies
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