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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1989 | 1 |
1992 | 2 |
1993 | 1 |
2024 | 0 |
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Page 1
Waardenburg syndrome type I in a child with deletion (2) (q35q36.2).
Am J Med Genet. 1992 Nov 15;44(5):699-700. doi: 10.1002/ajmg.1320440533.
Am J Med Genet. 1992.
PMID: 1481835
Review.
No abstract available.
Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy.
Lin SP, Petty EM, Gibson LH, Inserra J, Seashore MR, Yang-Feng TL.
Lin SP, et al.
Am J Med Genet. 1992 Nov 1;44(4):500-2. doi: 10.1002/ajmg.1320440424.
Am J Med Genet. 1992.
PMID: 1442895
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Gene for Waardenburg syndrome type I is located at 2q35, not at 2q37.3.
Ishikiriyama S.
Ishikiriyama S.
Am J Med Genet. 1993 Jun 15;46(5):608. doi: 10.1002/ajmg.1320460534.
Am J Med Genet. 1993.
PMID: 8322830
No abstract available.
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Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).
Ishikiriyama S, Tonoki H, Shibuya Y, Chin S, Harada N, Abe K, Niikawa N.
Ishikiriyama S, et al.
Am J Med Genet. 1989 Aug;33(4):505-7. doi: 10.1002/ajmg.1320330419.
Am J Med Genet. 1989.
PMID: 2596512
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