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December 1985
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
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.
Citation
Dorothy A. Gibbs, C.M. Headhouse-Benson, I.R. McFadyen, M.d'A. Crawfurd, R.W.E. Watts; Prenatal Diagnosis of The Lesch-Nyhan Syndrome using A Full Length cDNA Probe for the HPRT Gene. Clin Sci (Lond) 1 December 1985; 69 (s12): 26P. doi: https://doi.org/10.1042/cs069026P
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