Congenital Cranial Dysinnervation Disorders ☆

Author:

Bosley T.M.,Oystreck D.T.,Abu-Amero K.K.

Publisher

Elsevier

Reference64 articles.

1. Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder;Abu-Amero;Ophthalmic Genet.,2012

2. Xq26.3 Microdeletion in a male with Wildervanck syndrome;Abu-Amero;Ophthalmic Genet.,2013

3. Duane retraction syndrome associated with a small X chromosome deletion;Abu-Amero;Can. J. Neurol. Sci.,2016

4. Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family;Al-Baradie;Am. J. Hum. Genet.,2002

5. Patients with horizontal gaze palsy and progressive scoliosis due to ROBO3 E319K mutation have both uncrossed and crossed central nervous system pathways and perform normally on neuropsychological testing;Amoiridis;J. neurol. Neurosurg. Psychiatry,2006

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