Related references
Note: Only part of the references are listed.
Article
Genetics & Heredity
Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies
Leisha D. Nolen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Article
Genetics & Heredity
SOX2 anophthalmia syndrome
NK Ragge et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Share Paper
