Prenatal Diagnosis of The Lesch-Nyhan Syndrome using A Full Length cDNA Probe for the HPRT Gene

Gibbs, Dorothy A.; Headhouse-Benson, C.M.; McFadyen, I.R.; Crawfurd, M.d'A.; Watts, R.W.E.

doi:10.1042/cs069026P

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Conference Abstract| December 01 1985

Prenatal Diagnosis of The Lesch-Nyhan Syndrome using A Full Length cDNA Probe for the HPRT Gene

Dorothy A. Gibbs;

Dorothy A. Gibbs

¹ Division of Inherited Metabolic Diseases, MRC Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ

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C.M. Headhouse-Benson;

C.M. Headhouse-Benson

¹ Division of Inherited Metabolic Diseases, MRC Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ

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I.R. McFadyen;

I.R. McFadyen

² Section of Perinatal and Child Health, MRC Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ

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M.d'A. Crawfurd;

M.d'A. Crawfurd

¹ Division of Inherited Metabolic Diseases, MRC Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ

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R.W.E. Watts

¹ Division of Inherited Metabolic Diseases, MRC Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ

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Clin Sci (Lond) (1985) 69 (s12): 26P.

https://doi.org/10.1042/cs069026P

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