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Pregled bibliografske jedinice broj: 674879

Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability

Sansović, Ivona; Barišić, Ingeborg
Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability // European Journal of Human Genetics
Pariz, Francuska: Nature publishing group, 2013. str. 171-171 (poster, međunarodna recenzija, sažetak, znanstveni)

CROSBI ID: 674879 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability

Autori
Sansović, Ivona ; Barišić, Ingeborg

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
European Journal of Human Genetics / - : Nature publishing group, 2013, 171-171

Skup
European Human Genetics Conference

Mjesto i datum
Pariz, Francuska, 08.06.2013. - 11.06.2013

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
FMR1; AFF2

Sažetak
Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability

Izvorni jezik
Engleski



POVEZANOST RADA

Projekti:
072-1083107-0365 - Istraživanje epidemiologijskih i genetičkih osnova prirođenih mana (Barišić, Ingeborg, MZOS ) ( CroRIS)

Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta

Profili:

Avatar Url Ingeborg Barišić (autor)

Avatar Url Ivona Sansović (autor)

Citiraj ovu publikaciju:

Sansović, Ivona; Barišić, Ingeborg
Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability // European Journal of Human Genetics
Pariz, Francuska: Nature publishing group, 2013. str. 171-171 (poster, međunarodna recenzija, sažetak, znanstveni)
Sansović, I. & Barišić, I. (2013) Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability. U: European Journal of Human Genetics.
@article{article, author = {Sansovi\'{c}, Ivona and Bari\v{s}i\'{c}, Ingeborg}, year = {2013}, pages = {171-171}, keywords = {FMR1, AFF2}, title = {Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability}, keyword = {FMR1, AFF2}, publisher = {Nature publishing group}, publisherplace = {Pariz, Francuska} }
@article{article, author = {Sansovi\'{c}, Ivona and Bari\v{s}i\'{c}, Ingeborg}, year = {2013}, pages = {171-171}, keywords = {FMR1, AFF2}, title = {Detection of full mutation FMR1 and AFF2 alleles by Methylation- Specific Multiplex Ligation-dependent Probe Amplification method in male patients with intellectual disability}, keyword = {FMR1, AFF2}, publisher = {Nature publishing group}, publisherplace = {Pariz, Francuska} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE

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