DE69721889D1 - Pränatales Testverfahren für Down-Syndrom - Google Patents

Pränatales Testverfahren für Down-Syndrom

Info

Publication number
DE69721889D1
DE69721889D1 DE69721889T DE69721889T DE69721889D1 DE 69721889 D1 DE69721889 D1 DE 69721889D1 DE 69721889 T DE69721889 T DE 69721889T DE 69721889 T DE69721889 T DE 69721889T DE 69721889 D1 DE69721889 D1 DE 69721889D1
Authority
DE
Germany
Prior art keywords
stage
marker
abnormality
test procedure
down syndrome
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
DE69721889T
Other languages
English (en)
Other versions
DE69721889T2 (de
Inventor
Christopher John Davies
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ortho Clinical Diagnostics Ltd
Original Assignee
Ortho Clinical Diagnostics Ltd
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 Ortho Clinical Diagnostics Ltd filed Critical Ortho Clinical Diagnostics Ltd
Publication of DE69721889D1 publication Critical patent/DE69721889D1/de
Application granted granted Critical
Publication of DE69721889T2 publication Critical patent/DE69721889T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/74—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
    • G01N33/76—Human chorionic gonadotropin including luteinising hormone, follicle stimulating hormone, thyroid stimulating hormone or their receptors

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Endocrinology (AREA)
  • Biomedical Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Food Science & Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Reproductive Health (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Eye Examination Apparatus (AREA)
  • Investigating Strength Of Materials By Application Of Mechanical Stress (AREA)
  • Peptides Or Proteins (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Surgical Instruments (AREA)
DE69721889T 1996-03-25 1997-03-24 Pränatales Testverfahren für Down-Syndrom Expired - Lifetime DE69721889T2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9606261.7A GB9606261D0 (en) 1996-03-25 1996-03-25 Prenatal screening for fetal abnormalities
GB9606261 1996-03-25

Publications (2)

Publication Number Publication Date
DE69721889D1 true DE69721889D1 (de) 2003-06-18
DE69721889T2 DE69721889T2 (de) 2004-06-17

Family

ID=10790985

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69721889T Expired - Lifetime DE69721889T2 (de) 1996-03-25 1997-03-24 Pränatales Testverfahren für Down-Syndrom

Country Status (10)

Country Link
US (1) US5906944A (de)
EP (1) EP0800085B1 (de)
JP (1) JPH1019889A (de)
AT (1) ATE240525T1 (de)
AU (1) AU723148B2 (de)
DE (1) DE69721889T2 (de)
DK (1) DK0800085T3 (de)
ES (1) ES2198532T3 (de)
GB (1) GB9606261D0 (de)
PT (1) PT800085E (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0317476D0 (en) * 2003-07-25 2003-08-27 Wright David E Methods and apparatus for screening for chromosomal abnormalities
US7315787B2 (en) * 2003-10-07 2008-01-01 Ntd Laboratories, Inc. Multi-marker screening protocol for fetal abnormalities
US20060046274A1 (en) * 2004-08-31 2006-03-02 Repromedix Corporation And Shimon Segal Inhibin-A: a marker for differentiation, diagnosing and screening abnormal pregnancies

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4454232A (en) * 1982-06-07 1984-06-12 Bio-Rad Laboratories, Inc. Estriol assay
AU599373B2 (en) * 1986-03-13 1990-07-19 Biotechnology Australia Proprietary Limited Method of assay of inhibin
US4874693A (en) * 1986-10-10 1989-10-17 Mark Bogart Method for assessing placental dysfunction
ATE91182T1 (de) * 1987-07-09 1993-07-15 3I Res Expl Ltd Praenatales screening fuer downs-syndrom.
US5506150A (en) * 1987-07-09 1996-04-09 3I Research Exploitation Limited Prenatal screening for down's syndrome
JP2643968B2 (ja) * 1988-02-03 1997-08-25 サントリー株式会社 Ｋｅｘ２エンドプロテアーゼ及びその製造方法
US5252489A (en) * 1989-01-17 1993-10-12 Macri James N Down syndrome screening method utilizing dried blood samples
US5324667A (en) * 1989-01-17 1994-06-28 Macri James N Method for detecting down sydrown by non-invasive maternal blood screening
DE69026153T3 (de) * 1989-01-17 2005-05-12 Macri, James N. Downsyndrom-screening-methode
US5258907A (en) * 1989-01-17 1993-11-02 Macri James N Method and apparatus for detecting down syndrome by non-invasive maternal blood screening
US5316953A (en) * 1989-01-17 1994-05-31 Macri James N Screening method for detecting fetal chromosal abnormalities
US5100806A (en) * 1989-03-24 1992-03-31 Macri James N Method for detecting Edwards syndrome
GB9224965D0 (en) * 1992-11-28 1993-01-20 Kodak Ltd Antenatal screening for chromosomal abnormalities
WO1994021686A1 (en) * 1993-03-19 1994-09-29 Northern Sydney Area Health Service Papp-a, its immunodetection and uses
GB9306354D0 (en) * 1993-03-26 1993-05-19 Kodak Ltd Antenatal screening for chromosomal abnormalities
GB9315230D0 (en) * 1993-07-22 1993-09-08 Kodak Ltd Antenatal screening for chromosomal abnormalities
GB9416415D0 (en) * 1994-08-13 1994-10-05 Kodak Ltd Antenatel screening for pregnacy abnormalities
US5716853A (en) * 1995-07-07 1998-02-10 Chiron Diagnostics Corporation Prenatal down syndrome screening with assays specific for UGP

Also Published As

Publication number Publication date
ES2198532T3 (es) 2004-02-01
EP0800085A3 (de) 1999-03-17
PT800085E (pt) 2003-09-30
AU1652597A (en) 1997-10-02
JPH1019889A (ja) 1998-01-23
DK0800085T3 (da) 2003-09-08
ATE240525T1 (de) 2003-05-15
EP0800085A2 (de) 1997-10-08
DE69721889T2 (de) 2004-06-17
AU723148B2 (en) 2000-08-17
EP0800085B1 (de) 2003-05-14
GB9606261D0 (en) 1996-05-29
US5906944A (en) 1999-05-25

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8328 Change in the person/name/address of the agent

Representative=s name: BOEHMERT & BOEHMERT, 28209 BREMEN