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Year | Number of Results |
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1992 | 1 |
1993 | 1 |
2024 | 0 |
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Screening for molecular pathologies in Lesch-Nyhan syndrome.
Hum Mutat. 1993;2(2):127-30. doi: 10.1002/humu.1380020212.
Hum Mutat. 1993.
PMID: 8318989
A review of the molecular basis of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.
Sculley DG, Dawson PA, Emmerson BT, Gordon RB.
Sculley DG, et al.
Hum Genet. 1992 Nov;90(3):195-207. doi: 10.1007/BF00220062.
Hum Genet. 1992.
PMID: 1487231
Review.
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