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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1994 | 1 |
1996 | 1 |
2024 | 0 |
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Page 1
Who is a carrier? Detection of unsuspected mutations in 21-hydroxylase deficiency.
Am J Med Genet. 1996 Jan 2;61(1):2-9. doi: 10.1002/(SICI)1096-8628(19960102)61:1<2::AID-AJMG1>3.0.CO;2-1.
Am J Med Genet. 1996.
PMID: 8741909
Molecular diagnosis of 21-hydroxylase deficiency: detection of four mutations on a single gel.
Siegel SF, Hoffman EP, Trucco M.
Siegel SF, et al.
Biochem Med Metab Biol. 1994 Feb;51(1):66-73. doi: 10.1006/bmmb.1994.1009.
Biochem Med Metab Biol. 1994.
PMID: 8192919
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Pituitary stalk and ectopic hyperintense T1 signal on magnetic resonance imaging. Implications for anterior pituitary dysfunction.
Ultmann MC, Siegel SF, Hirsch WL, Finegold DN, Foley TP Jr.
Ultmann MC, et al.
Am J Dis Child. 1993 Jun;147(6):647-52. doi: 10.1001/archpedi.1993.02160300053022.
Am J Dis Child. 1993.
PMID: 8506833
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