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Academic Journal

Neuropsychological Deficits in Autosomal Dominant Cerebellar Ataxia: An Examination of Three Affected Family Members, One with Psychosis.

Authors : Morton, Nicola S. Gray David V. James Graham Pickup Paul Gilluley Sean Spence Andrew Vidgen Nick

Source: Cognitive Neuropsychiatry. Nov98, Vol. 3 Issue 4, p259-268. 10p.

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Academic Journal

Glucose intolerance in familial combined hyperlipidaemia.

Authors : Vakkilainen; Porkka; Nuotio

Source: European Journal of Clinical Investigation. Jan1998, Vol. 28 Issue 1, p24-32. 9p.

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Academic Journal

Family histories of children with SLI who show extended optional infinitives.

Authors : Rice ML (AUTHOR); Haney KR (AUTHOR); Wexler K (AUTHOR)

Source: Journal of Speech, Language & Hearing Research. Apr1998, Vol. 41 Issue 2, p419-432. 14p.

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Academic Journal

Phenotypic expression of autosomal dominant retinitis pigmentosain a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.

Authors : Ekström, Ulf; Ponjavic, Vesna; Abrahamson, Magnus

Source: Ophthalmic Genetics. Mar1998, Vol. 19 Issue 1, p27. 11p.

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Academic Journal

Genetic and functional studies of a germline TP53 splicing mutation in a Li–Fraumeni-like family.

Authors : Varley, J M; Chapman, P; McGown, G

Source: Oncogene. 6/25/98, Vol. 16 Issue 25, p3291. 8p.

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Academic Journal

Identification of a C → T Mutation in the Reactive-Site Coding Region of the C1-Inhibitor Gene and its Detection by an Improved Mutation-Specific Polymerase Chain Reaction Method.

Authors : Nielsen; Fure; Winge

Source: Scandinavian Journal of Immunology. Mar1998, Vol. 47 Issue 3. 2 Diagrams.

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فلترة النتائج

Neuropsychological Deficits in Autosomal Dominant Cerebellar Ataxia: An Examination of Three Affected Family Members, One with Psychosis.

Glucose intolerance in familial combined hyperlipidaemia.

Family histories of children with SLI who show extended optional infinitives.

Phenotypic expression of autosomal dominant retinitis pigmentosain a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.

Genetic and functional studies of a germline TP53 splicing mutation in a Li–Fraumeni-like family.

Identification of a C → T Mutation in the Reactive-Site Coding Region of the C1-Inhibitor Gene and its Detection by an Improved Mutation-Specific Polymerase Chain Reaction Method.

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