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Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder.
- Source :
-
Neurosciences (Riyadh, Saudi Arabia) [Neurosciences (Riyadh)] 2016 Jan; Vol. 21 (1), pp. 72-4. - Publication Year :
- 2016
- Subjects :
- Blepharoptosis congenital
Child
Cleft Palate genetics
Cranial Nerve Diseases congenital
Esotropia congenital
Female
Humans
Polydactyly genetics
Pulmonary Valve Stenosis congenital
Pulmonary Valve Stenosis genetics
Strabismus congenital
Strabismus genetics
Abnormalities, Multiple genetics
Blepharoptosis genetics
Chromosomes, Human, Pair 6
Cranial Nerve Diseases genetics
Cullin Proteins genetics
Esotropia genetics
Gene Deletion
Subjects
Details
- Language :
- English
- ISSN :
- 1319-6138
- Volume :
- 21
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Neurosciences (Riyadh, Saudi Arabia)
- Publication Type :
- Academic Journal
- Accession number :
- 26818173
- Full Text :
- https://doi.org/10.17712/nsj.2016.1.20150098