Results 61 to 70 of about 462 (99)

Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia. [PDF]

open access: yesJ Med Genet, 2004
Wieland I   +5 more
europepmc   +1 more source

Branchio-oto-renal syndrome: a narrative review. [PDF]

open access: yesChild Kidney Dis
Kumarasamy G   +4 more
europepmc   +1 more source

Imaging of the Hyrtl Fissure: A Rare Cause of Congenital CSF Otorrhea. [PDF]

open access: yesAJNR Am J Neuroradiol
Clarke JE   +5 more
europepmc   +1 more source

Evaluation of Cochlear Basal Turn Patency in Children with Hearing Loss. [PDF]

open access: yesJ Assoc Res Otolaryngol
Aramendi M   +6 more
europepmc   +1 more source

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