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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1952 1
1956 1
1959 1
1968 1
1975 1
1977 1
1980 1
1981 2
1982 3
1984 1
1987 1
1988 1
1992 1
1993 4
1994 8
1995 6
1996 3
1997 5
1998 1
1999 3
2000 2
2001 6
2002 1
2003 2
2024 0

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PubMed (OMIM) for id: 1324

57 results

Results by year

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Page 1
Addison's disease in two brothers.
MEAKIN JW, NELSON DH, THORN GW. MEAKIN JW, et al. J Clin Endocrinol Metab. 1959 Jun;19(6):726-31. doi: 10.1210/jcem-19-6-726. J Clin Endocrinol Metab. 1959. PMID: 13654502 No abstract available.
Familial occurrence of Addison's disease.
BROCHNER-MORTENSEN K. BROCHNER-MORTENSEN K. Acta Med Scand. 1956 Dec 22;156(3):205-9. doi: 10.1111/j.0954-6820.1956.tb00077.x. Acta Med Scand. 1956. PMID: 13381433 No abstract available.
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, Steinberg SJ. Corzo D, et al. Am J Hum Genet. 2002 Jun;70(6):1520-31. doi: 10.1086/340849. Epub 2002 Apr 29. Am J Hum Genet. 2002. PMID: 11992258 Free PMC article.
57 results