Aplasia cutis congenita of the scalp in a female infant with anophthalmia/microphthalmia-esophageal atresia syndrome negative for SOX2 mutation.
PMID 23463581 · American journal of medical genetics. Part A · 2013 · DOI 10.1002/ajmg.a.35854
Authors: J Román Corona-Rivera; Juan Carlos Zenteno; Erika Pelcastre-Luna; Karla Miguel-Jiménez; Rafael L Aguirre-Guillén; Jesús Cabral-Macías; Christian Peña-Padilla; Lucina Bobadilla-Morales; Alfredo Corona-Rivera
Abstract
No abstract published for this record.
Ectodermal Dysplasia; Esophageal Atresia; Female; Humans; Infant; Microphthalmos; Mutation; Nervous System Malformations; SOXB1 Transcription Factors; Scalp
Cite
J Román Corona-Rivera; Juan Carlos Zenteno; Erika Pelcastre-Luna; Karla Miguel-Jiménez; Rafael L Aguirre-Guillén; Jesús Cabral-Macías; Christian Peña-Padilla; Lucina Bobadilla-Morales; Alfredo Corona-Rivera. Aplasia cutis congenita of the scalp in a female infant with anophthalmia/microphthalmia-esophageal atresia syndrome negative for SOX2 mutation. American journal of medical genetics. Part A (2013). PMID 23463581. DOI 10.1002/ajmg.a.35854.