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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1986 | 1 |
1996 | 1 |
2000 | 1 |
2024 | 0 |
PubMed for Bookshelf ID: 2983778
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Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
Am J Med Genet. 2000 Apr 10;91(4):313-7.
Am J Med Genet. 2000.
PMID: 10766989
A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspring.
Tuck-Muller CM, Varela M, Li S, Pridjian G, Chen H, Wertelecki W.
Tuck-Muller CM, et al.
Am J Med Genet. 1996 May 17;63(2):392-5. doi: 10.1002/(SICI)1096-8628(19960517)63:2<392::AID-AJMG13>3.0.CO;2-F.
Am J Med Genet. 1996.
PMID: 8725792
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Prometaphase chromosome analysis as a routine diagnostic technique.
Barnes IC, Maltby EL.
Barnes IC, et al.
Clin Genet. 1986 May;29(5):378-83. doi: 10.1111/j.1399-0004.1986.tb00508.x.
Clin Genet. 1986.
PMID: 3742844
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