DE69225797D1 - Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x - Google Patents

Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x

Info

Publication number
DE69225797D1
DE69225797D1 DE69225797T DE69225797T DE69225797D1 DE 69225797 D1 DE69225797 D1 DE 69225797D1 DE 69225797 T DE69225797 T DE 69225797T DE 69225797 T DE69225797 T DE 69225797T DE 69225797 D1 DE69225797 D1 DE 69225797D1
Authority
DE
Germany
Prior art keywords
sensitive
nucleic acid
acid fragment
mental
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
DE69225797T
Other languages
English (en)
Other versions
DE69225797T2 (de
Inventor
Jean-Louis Mandel
Francois Rousseau
Anne Vincent
Dominique Heitz
Isabelle Oberle
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.)
Institut National de la Sante et de la Recherche Medicale INSERM
Original Assignee
Institut National de la Sante et de la Recherche Medicale INSERM
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 Institut National de la Sante et de la Recherche Medicale INSERM filed Critical Institut National de la Sante et de la Recherche Medicale INSERM
Priority claimed from PCT/FR1992/000145 external-priority patent/WO1992014840A1/fr
Application granted granted Critical
Publication of DE69225797D1 publication Critical patent/DE69225797D1/de
Publication of DE69225797T2 publication Critical patent/DE69225797T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • C12Q2600/154—Methylation 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
    • C12Q2600/156—Polymorphic or mutational markers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Analytical Chemistry (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Pathology (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
DE69225797T 1991-02-13 1992-02-13 Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x Expired - Lifetime DE69225797T2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9101684A FR2672618B1 (fr) 1991-02-13 1991-02-13 Fragment d'acide nucleique de la region du chromosome x implique dans le syndrome x fragile, sonde nucleotidique et procede pour le diagnostic du retard mental avec x fragile.
PCT/FR1992/000145 WO1992014840A1 (fr) 1991-02-13 1992-02-13 Fragment d'acide nucleique de la region du chromosome x implique dans le syndrome x fragile, sonde nucleotidique et procede pour le diagnostic du retard mental avec x fragile

Publications (2)

Publication Number Publication Date
DE69225797D1 true DE69225797D1 (de) 1998-07-09
DE69225797T2 DE69225797T2 (de) 1999-02-04

Family

ID=9409670

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69225797T Expired - Lifetime DE69225797T2 (de) 1991-02-13 1992-02-13 Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x

Country Status (8)

Country Link
EP (1) EP0580621B1 (de)
JP (1) JPH06507310A (de)
AT (1) ATE166925T1 (de)
AU (1) AU671418B2 (de)
CA (1) CA2104110C (de)
DE (1) DE69225797T2 (de)
ES (1) ES2118130T3 (de)
FR (1) FR2672618B1 (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10019058A1 (de) * 2000-04-06 2001-12-20 Epigenomics Ag Detektion von Variationen des DNA-Methylierungsprofils
RU2011142773A (ru) 2009-03-24 2013-04-27 Эсьюраджен, Инк. Методы пцр для характеристики 5,-нетранслируемого участка генов fmr1 и fmr2
EP2888688B1 (de) 2012-07-20 2019-09-04 Asuragen, INC. Umfassende fmr1-genotypisierung
CN110923305B (zh) * 2019-11-25 2023-12-29 广州市达瑞生物技术股份有限公司 一种适用于脆性X综合征southern blot印迹杂交检测的DNA分子量标准

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2578847A1 (fr) * 1985-03-13 1986-09-19 Centre Nat Rech Scient Sonde adn destinee au diagnostic antenatal de certaines anomalies chromosomiques
GB8825530D0 (en) * 1988-11-01 1988-12-07 Medical Res Council Probe
GB8928029D0 (en) * 1989-12-12 1990-02-14 Medical Res Council Probe
EP0724646B1 (de) * 1991-01-04 2001-06-27 Washington University Mit isoliertem empfindlichem x-syndrom verbundene dns-sequenzen

Also Published As

Publication number Publication date
JPH06507310A (ja) 1994-08-25
DE69225797T2 (de) 1999-02-04
FR2672618A1 (fr) 1992-08-14
ES2118130T3 (es) 1998-09-16
EP0580621B1 (de) 1998-06-03
CA2104110C (fr) 2003-12-09
CA2104110A1 (fr) 1992-08-14
AU1413692A (en) 1992-09-15
ATE166925T1 (de) 1998-06-15
EP0580621A1 (de) 1994-02-02
FR2672618B1 (fr) 1994-12-02
AU671418B2 (en) 1996-08-29

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