Item request has been placed!
×
Item request cannot be made.
×
Processing Request
Exome sequencing reveals novel homozygous FOXE3 mutation in microphthalmos with staphylomatous malformation.
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
- معلومة اضافية
- المصدر:
Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE
- بيانات النشر:
Publication: London : Informa Healthcare
Original Publication: Buren, The Netherlands : Aeolus Press, c1994-
- الموضوع:
- الرقم المعرف:
0 (FOXE3 protein, human)
0 (Forkhead Transcription Factors)
- الموضوع:
Date Created: 20160927 Date Completed: 20171117 Latest Revision: 20220330
- الموضوع:
20250114
- الرقم المعرف:
10.1080/13816810.2016.1217549
- الرقم المعرف:
27669367
No Comments.