HK1126254A1 - Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms - Google Patents

Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms

Info

Publication number
HK1126254A1
HK1126254A1 HK09104895.9A HK09104895A HK1126254A1 HK 1126254 A1 HK1126254 A1 HK 1126254A1 HK 09104895 A HK09104895 A HK 09104895A HK 1126254 A1 HK1126254 A1 HK 1126254A1
Authority
HK
Hong Kong
Prior art keywords
single nucleotide
nucleotide polymorphisms
fetal chromosomal
chromosomal abnormalities
tandem single
Prior art date
Application number
HK09104895.9A
Other languages
English (en)
Inventor
Aoy Tomita Mitchell
Michael Mitchell
Original Assignee
Univ Louisville Res Found
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Univ Louisville Res Found filed Critical Univ Louisville Res Found
Publication of HK1126254A1 publication Critical patent/HK1126254A1/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/156—Polymorphic or mutational markers
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/172—Haplotypes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
    • Y10T436/142222—Hetero-O [e.g., ascorbic acid, etc.]
    • Y10T436/143333—Saccharide [e.g., DNA, etc.]
HK09104895.9A 2006-02-28 2009-06-01 Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms HK1126254A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US77786506P 2006-02-28 2006-02-28
PCT/US2007/005399 WO2007100911A2 (en) 2006-02-28 2007-02-28 Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms

Publications (1)

Publication Number Publication Date
HK1126254A1 true HK1126254A1 (en) 2009-08-28

Family

ID=38293156

Family Applications (1)

Application Number Title Priority Date Filing Date
HK09104895.9A HK1126254A1 (en) 2006-02-28 2009-06-01 Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms

Country Status (10)

Country Link
US (3) US7799531B2 (xx)
EP (2) EP2351858B1 (xx)
AT (1) ATE508209T1 (xx)
AU (1) AU2007220991C1 (xx)
CA (1) CA2647793C (xx)
DE (1) DE602007014335D1 (xx)
DK (2) DK1996728T3 (xx)
HK (1) HK1126254A1 (xx)
SI (2) SI1996728T1 (xx)
WO (1) WO2007100911A2 (xx)

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US8663921B2 (en) 2014-03-04
EP2351858B1 (en) 2014-12-31
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DK1996728T3 (da) 2011-08-15
US20080020390A1 (en) 2008-01-24
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ATE508209T1 (de) 2011-05-15
SI2351858T1 (sl) 2015-06-30
US7799531B2 (en) 2010-09-21
US20110059451A1 (en) 2011-03-10
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US20130231252A1 (en) 2013-09-05
US9181586B2 (en) 2015-11-10
EP2351858A1 (en) 2011-08-03
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CA2647793C (en) 2016-07-05
AU2007220991C1 (en) 2013-08-15
AU2007220991A1 (en) 2007-09-07

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