Literature DB >> 4747812

An atypical case of hypoxanthine-guanine phosphoribosyltransferase deficiency (Lesch-Nyhan syndrome). II. Genetic studies.

C H de Bruyn, T L Oei, R A Geerdink, E J Lommen.   

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Year:  1973        PMID： 4747812     DOI： 10.1111/j.1399-0004.1973.tb01931.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

1.  Differential responses to mitogen stimulation in lymphocytes from normal individuals and Lesch-Nyhan patients: influence of the bicarbonate buffer system.

Authors:  P Gausset; E Vamos; G Delespesse; S Kulakowski; J Duchateau; C de Bruyn
Journal:  Clin Exp Immunol       Date:  1980-11       Impact factor: 4.330

Review 2.  Hypoxanthine-guanine phosphoribosyl transferase deficiency.

Authors:  C H de Bruyn
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

3.  Molecular and tissue-specific heterogeneity in HPRT deficiency.

Authors:  M P Uitendaal; C H de Bruyn; T L Oei; P Hösli
Journal:  Biochem Genet       Date:  1978-12       Impact factor: 1.890
  3 in total

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