2006.

Extending genotype-phenotype studies of Rett syndrome using the British Isles Rett Survey database and the Rett Syndrome Behaviour Question.

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Reference: Dr Mark Bailey Abstract: n.a PROJECT DETAILS  beginning: 2004. end: 2006. Country of research: United Kingdom Counry of funding source: United Kingdom Funding organization: Rett UK Financing: PRIVATE FUNDERS – 0 € hyperlink

Fundacion La Marato de TV3ﾠ

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Reference: 115 Abstract: n.a PROJECT DETAILS  beginning: 2005. end: 2006. Country of research: Spain Counry of funding source: Spain Funding organization: Fundacion La Marato de TV3ﾠ Financing: PRIVATE FUNDERS – 0 € hyperlink

A ChIP-on-chip system for dissecting genetic pathways involved in developmental language disorders

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Reference: Fisher Simon Abstract: The Fisher lab has previously reported that mutations of a gene, called FOXP2, cause a severe developmental communication disorder. FOXP2 abnormalities lead to problems with articulating speech, accompanied by impairment in many aspects of language ability. The protein made by FOXP2 controls the behavior of cells by binding to DNA and … Read more

Extending genotype-phenotype studies of Rett syndrome using the British Isles Rett Survey database and the Rett Syndrome Behaviour Question

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Reference: Dr MarkﾠBailey Abstract: n.a PROJECT DETAILS  beginning: 2005. end: 2006. Country of research: United Kingdom Counry of funding source: United Kingdom Funding organization: Rett Syndrome Association Scotland Financing: PRIVATE FUNDERS – 0 € hyperlink

Cell lines and DNA bank of Rett syndrome and other X-linked mental retardation

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Reference: GTF05005 Abstract: Mental retardation (MR) is the most frequent cause of serious handicap in humans and an important health-care problem throughout the world. It is estimated to occur in about 1-3% of the general population. It is calculated that X-linked mental retardation (XLMR) may account for about 20ﾖ25% of mentally retarded males. The number … Read more

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