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Items: 2

1.
Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation
N Harada, E Hatchwell, N Okamoto, M Tsukahara, K Kurosawa, H Kawame, T Kondoh, H Ohashi, R Tsukino, Y Kondoh, O Shimokawa, T Ida, T Nagai, Y Fukushima, K Yoshiura, N Niikawa, N Matsumoto
J Med Genet. 2004 Feb; 41(2): 130–136. doi: 10.1136/jmg.2003.014639
PMCID:
PMC1735677
SummaryPDF–791K
2.
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.
R Tupler, L Bortotto, E M Bühler, M Alkan, N J Malik, N Bösch-Al Jadooa, L Memo, P Maraschio
J Med Genet. 1992 Jan; 29(1): 53–55. doi: 10.1136/jmg.29.1.53
PMCID:
PMC1015823
SummaryPage BrowsePDF–671K

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