Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder

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Bibliographische Detailangaben
Veröffentlicht in:	Neurosciences 2016-01, Vol.21 (1), p.72-74
Hauptverfasser:	Abu-Amero, Khaled K, Kondkar, Altaf A, Hellani, Ali M, Bosley, Thomas M, Khan, Arif O
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - genetics Blepharoptosis - congenital Blepharoptosis - genetics Child Chromosomes, Human, Pair 6 Cleft Palate - genetics Clinical Note Cranial Nerve Diseases - congenital Cranial Nerve Diseases - genetics Cullin Proteins - genetics Cytogenetics Esotropia - congenital Esotropia - genetics Female Gene Deletion Genetic aspects Genetic disorders Humans Medical schools Polydactyly - genetics Pulmonary Valve Stenosis - congenital Pulmonary Valve Stenosis - genetics Strabismus - congenital Strabismus - genetics
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