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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1987 | 1 |
1988 | 1 |
1998 | 1 |
2009 | 1 |
2013 | 1 |
2015 | 1 |
2024 | 0 |
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Page 1
High-resolution SNP microarray investigation of copy number variations on chromosome 18 in a control cohort.
Cytogenet Genome Res. 2013;141(1):16-25. doi: 10.1159/000350767. Epub 2013 Apr 26.
Cytogenet Genome Res. 2013.
PMID: 23635498
A comprehensive set of idiograms representing all interpretive levels of resolution: ISCN (2009).
Chia NL.
Chia NL.
Cytogenet Genome Res. 2009;125(2):162-4. doi: 10.1159/000227842. Epub 2009 Aug 31.
Cytogenet Genome Res. 2009.
PMID: 19729921
No abstract available.
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Trisomy (1q)(q42----qter): confirmation of a syndrome.
Chia NL, Bousfield LR, Poon CC, Trudinger BJ.
Chia NL, et al.
Clin Genet. 1988 Oct;34(4):224-9.
Clin Genet. 1988.
PMID: 3233776
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A case report of a de novo tandem duplication (5p) (p14----pter).
Chia NL, Bousfield LR, Johnson BH.
Chia NL, et al.
Clin Genet. 1987 Feb;31(2):65-9. doi: 10.1111/j.1399-0004.1987.tb02771.x.
Clin Genet. 1987.
PMID: 3829442
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Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.
Mowat DR, Croaker GD, Cass DT, Kerr BA, Chaitow J, Adès LC, Chia NL, Wilson MJ.
Mowat DR, et al. Among authors: chia nl.
J Med Genet. 1998 Aug;35(8):617-23. doi: 10.1136/jmg.35.8.617.
J Med Genet. 1998.
PMID: 9719364
Free PMC article.
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Detection of segmental chromosome copy number gains by improved fluorescence in situ hybridization techniques.
Chia NL, Slater HR, Potter JM.
Chia NL, et al.
J Assoc Genet Technol. 2015;41(1):5-11.
J Assoc Genet Technol. 2015.
PMID: 26030083
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