(Q43705955)

26 November 2017

Preliminary evidence for a cognitive phenotype in Barth syndrome (English)

1 reference

26 November 2017

1 reference

Mazzocco MM

1

1 reference

PubMed ID

11503166

26 November 2017

Kelley RI

series ordinal

2

1 reference

26 November 2017

1 September 2001

1 reference

American Journal of Medical Genetics Part A

26 November 2017

1 reference

26 November 2017

102

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26 November 2017

4

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26 November 2017

372-378

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Molecular-neurobehavioral associations in females with the fragile X full mutation.

26 November 2017

1 reference

Early developmental trajectories of males with fragile X syndrome.

21 January 2018

1 reference

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

21 January 2018

1 reference

A novel X-linked gene, G4.5. is responsible for Barth syndrome

21 January 2018

1 reference

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome

21 January 2018

1 reference

Barth syndrome: clinical observations and genetic linkage studies.

21 January 2018

1 reference

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

21 January 2018

1 reference

Rapid "automatized" naming (R.A.N): dyslexia differentiated from other learning disabilities

21 January 2018

1 reference

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome

21 January 2018

1 reference

Multiple syndromes of 3-methylglutaconic aciduria

21 January 2018

1 reference

Mutation characterization and genotype-phenotype correlation in Barth syndrome

21 January 2018

1 reference

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

21 January 2018

1 reference

X chromosome inactivation in carriers of Barth syndrome

21 January 2018

1 reference

Contribution of the FMR1 gene mutation to human intellectual dysfunction

21 January 2018

1 reference

The psychoeducational characteristics of children with Turner syndrome.

21 January 2018

1 reference

Neuropsychology of early-treated phenylketonuria: specific executive function deficits

21 January 2018

1 reference

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

21 January 2018

1 reference

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism

21 January 2018

1 reference

Specific arithmetic calculation deficits in children with Turner syndrome

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/AJMG.1487

1 reference

26 November 2017

1 reference

PubMed ID

11503166