Methods for clinical diagnosis

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C435S091100, C435S018000, C435S019000, C435S040500, C435S040510, C536S023100, C536S023500

Reexamination Certificate

active

10257923

ABSTRACT:
A method for the identification of human foetal cell nuclei is provided wherein the method involves subjecting chromosomes of cell nuclei to exonucleolytic digestion by an enzyme so as to remove end regions of each chromosome; and detecting the presence of a DNA sequence remaining in foetal DNA but absent from maternal DNA as a result of the digestion process. Once identified, the foetal DNA can be subject to diagnosis for example to detect chromosomal abnormalities.

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patent: 6136540 (2000-10-01), Tsipouras et al.
patent: 0 430 402 (1991-06-01), None
patent: 94/02646 (1994-02-01), None
patent: 98/39474 (1998-09-01), None
Youngren et al, “Sychrony in telomere length of human fetus”, Hum. Genet., (1988); pp. 640-643.
Iwama et al, “Telomeric length and telmoerase activity vary with age in peripheral blood cells obtained from normal individuals”, Hum. Genet., (1998), pp. 397-402.
Verma et al., Lancet (1998) 352, 9-12.
Poon et al., Research Letters (2000) 356, 1819-1820.

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