๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Bart syndrome: Association with epidermolysis bullosa and aplasia cutis

Book ID
116586604
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
43 KB
Volume
62
Category
Article
ISSN
1097-6787

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Aplasia cutis congenita and/or epidermol
Aplasia cutis congenita and/or epidermolysis bullosa
โœ Vivona, Giuseppa ;Frontali, Marina ;Di Nunzio, M. Lucia ;Vendemiati, Antonio ;Op ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 451 KB
Epidermolysis bullosa, pyloric atresia,
Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: Histopathological delineation of an autosomal recessive disease
โœ Maman, Eran; Maor, Esther; Kachko, Leonid; Carmi, Rivka ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 84 KB ๐Ÿ‘ 2 views

The simultaneous appearance of epidermolysis bullosa and pyloric atresia (EB-PA) is recognized as an autosomal recessive disease; however, the coappearance of EB-PA and aplasia cutis congenita (ACC) has not been delineated as a defined entity. The aim of this study was to analyze clinically and hist

Deletion of the first pair of fibronecti
Deletion of the first pair of fibronectin type III repeats of the integrin ฮฒ-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients
โœ Ramon Y. Birnbaum; Daniella Landau; Khalil Elbedour; Rivka Ofir; Ohad S. Birk; R ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 147 KB ๐Ÿ‘ 1 views

Deletion of the first pair of fibronectin type III repeats of the integrin b-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients.