Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.

Author:

King M D,Dudgeon J,Stephenson J B

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference38 articles.

1. Familial agenesis of the cerebellar vermis;Joubert, M.; Eisenring, J.; Robb, J.P.; Andermann, F.;Neurology,1969

2. Defectos Vermianos; retraso mental; movimientos anormales y alteraciones dcl ritmo respiratorio;Santolaya, J.M.; Pascual-Castroviejo, I.;Rev Neurol (Spain),1974

3. Joubert syndrome: episodic hyperpnoea, anormal eye movements retardation and ataxia, associated with dysplasia of the cerebellar vermis;Boltshauser, E.; Isler, W.;Neuropediatrie,1977

4. Vermian agenesis and unsegmented midbrain tectum;Calogero, J.A.;J Neurosurg,1977

5. Joubert syndrome associated with Leber's congenital amaurosis. (in Japanese);Tomita, H.; Ohno, K.; Tamai, A.;Brain Dev,1979

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