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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1983 | 1 |
1987 | 1 |
1993 | 1 |
1994 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 167092
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Johnson-McMillin syndrome: report of another family.
Am J Med Genet. 1993 Oct 1;47(5):714-6. doi: 10.1002/ajmg.1320470526.
Am J Med Genet. 1993.
PMID: 8267002
Review.
Johnson-McMillin syndrome: report of another family.
Bankier A, Rose CM.
Bankier A, et al.
Am J Med Genet. 1994 Oct 1;52(4):493-4. doi: 10.1002/ajmg.1320520419.
Am J Med Genet. 1994.
PMID: 7747766
No abstract available.
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A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism.
Johnson VP, McMillin JM, Aceto T Jr, Bruins G.
Johnson VP, et al.
Am J Med Genet. 1983 Jul;15(3):497-506. doi: 10.1002/ajmg.1320150316.
Am J Med Genet. 1983.
PMID: 6881216
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Alopecia-anosmia-deafness-hypogonadism syndrome revisited: report of a new case.
Johnston K, Golabi M, Hall B, Ito M, Grix A.
Johnston K, et al.
Am J Med Genet. 1987 Apr;26(4):925-7. doi: 10.1002/ajmg.1320260422.
Am J Med Genet. 1987.
PMID: 3591836
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