Results 121 to 130 of about 11,195 (218)

VAX1mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of aVAX1phenotype in humans

open access: green, 2011
Anne Slavotinek   +11 more
openalex   +2 more sources

Chudley-McCullough syndrome: A report of a rare syndromic sensorineural hearing loss. [PDF]

open access: yesRadiol Case Rep
Ouqlani C   +6 more
europepmc   +1 more source

P15.03: Prenatal diagnosis and outcome of partial agenesis and hypoplasia of the corpus callosum [PDF]

open access: bronze, 2004
T. Ghi   +8 more
openalex   +1 more source

Rubinstein-Taybi syndrome with agenesis of corpus callosum.

open access: yesJ Pediatr Neurosci, 2015
Mishra S   +3 more
europepmc   +1 more source

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