Add to ORKGJoubert syndrome (JS) is an autosomal recessive disorder characterized by a malformation of the cerebellum, hypotonia, oculomotor apraxia, ataxia, abnormal breathing and mental retardation (for reviews, see Harris, 2007; Sharma et al., 2008). I
<p>Joubert Syndrome (JS) is a rare genetic disorder that affects the cerebellum and the brain ...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing th...
The clinical presentation of children with Joubert syndrome can include nonspecific features such as...
Research on children with Joubert syndrome has focused on brain structural abnormalities and associa...
Item does not contain fulltextBACKGROUND: The features of Joubert syndrome include hypotonia, ataxia...
PubMedID: 23692786Joubert syndrome (JS) is an autosomal recessive condition characterized by hypoton...
Joubert syndrome (JS) is a rare autosomal recessive central nervous system malformation characterize...
Joubert syndrome is a rare autosomal recessive disorder characterized by hyperpnoea and eye movement...
Joubert syndrome is an autosomal recessive condition characterized by hypotonia, ataxia, psychomotor...
Background Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterised by hypoton...
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome involving agenesis or dysg...
BACKGROUND Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterised by hypoto...
Background: Joubert syndrome (JS) is a recessively inherited disorder characterised by hypotonia at ...
Joubert Syndrome (JS) is a rare autosomal recessive or X-linked condition characterized by a peculia...
<p>Joubert Syndrome (JS) is a rare genetic disorder that affects the cerebellum and the brain ...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing th...
The clinical presentation of children with Joubert syndrome can include nonspecific features such as...
Research on children with Joubert syndrome has focused on brain structural abnormalities and associa...
Item does not contain fulltextBACKGROUND: The features of Joubert syndrome include hypotonia, ataxia...
PubMedID: 23692786Joubert syndrome (JS) is an autosomal recessive condition characterized by hypoton...
Joubert syndrome (JS) is a rare autosomal recessive central nervous system malformation characterize...
Joubert syndrome is a rare autosomal recessive disorder characterized by hyperpnoea and eye movement...
Joubert syndrome is an autosomal recessive condition characterized by hypotonia, ataxia, psychomotor...
Background Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterised by hypoton...
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome involving agenesis or dysg...
BACKGROUND Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterised by hypoto...
Background: Joubert syndrome (JS) is a recessively inherited disorder characterised by hypotonia at ...
Joubert Syndrome (JS) is a rare autosomal recessive or X-linked condition characterized by a peculia...
<p>Joubert Syndrome (JS) is a rare genetic disorder that affects the cerebellum and the brain ...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing th...