Léim chuig an ábhar
Logo APM
  • Logáil isteach
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
    • Māori
CASTA
  • Targeted sequencing identifies...
  • Luaigh é seo
  • Seol mar théacs é seo
  • Seol é seo mar r-phost
  • Priontáil
  • Easpórtáil taifead
    • Easpórtáil chuig RefWorks
    • Easpórtáil chuig EndNoteWeb
    • Easpórtáil chuig EndNote
  • Cuir le mo chuid Ceanán
  • Buan-nasc
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

Sábháilte in:
Sonraí bibleagrafaíochta
Príomhchruthaitheoirí: Holly A.F. Stessman, Bo Xiong, Bradley P. Coe, Tianyun Wang, Kendra Hoekzema, Michaela Fencková, Malin Kvarnung, Jennifer Gerdts, Sandy Trinh, Nele Cosemans, Laura Vives, Janice Lin, Tychele N. Turner, Gijs W.E. Santen, Claudia Ruivenkamp, Marjolein Kriek, Arie van Haeringen, Emmelien Aten, Kathryn Friend, Jan Liebelt, Christopher Barnett, Eric Haan, Marie Shaw, Jozef Gécz, Britt-Marie Anderlid, Ann Nordgren, Anna Lindstrand, Charles E. Schwartz, R. Frank Kooy, Geert Vandeweyer, Céline Helsmoortel, Corrado Romano, A Alberti, Mirella Vinci, Emanuela Avola, Stefania Giusto, Eric Courchesne, Tiziano Pramparo, Karen Pierce, Srinivasa Nalabolu, David G. Amaral, Ingrid E. Scheffer, Martin B. Delatycki, Paul J. Lockhart, Fereydoun Hormozdiari, Benjamin Harich, Anna Castells‐Nobau, Kun Xia, Hilde Peeters, Magnus Nordenskjöld, Annette Schenck, Raphael Bernier, Evan E. Eichler
Formáid: Artigo
Teanga:Béarla
Foilsithe / Cruthaithe: 2017
Rochtain ar líne:https://doi.org/10.1038/ng.3792
Clibeanna: Cuir clib leis
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
  • Stoc
  • Cur síos
  • Tráchtanna
  • Míreanna comhchosúla
  • Amharc foirne

Ar líne

https://doi.org/10.1038/ng.3792

Míreanna comhchosúla

  • Targeted sequencing identifies 91 neurodevelopmental disorder risk genes with autism and developmental disability biases
    de réir: Stessman, Holly A. F., et al.
    Foilsithe / Cruthaithe: (2017)
  • Hotspots of missense mutation identify novel neurodevelopmental disorder genes and functional domains
    de réir: Geisheker, Madeleine R., et al.
    Foilsithe / Cruthaithe: (2017)
  • Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
    de réir: Madeleine R. Geisheker, et al.
    Foilsithe / Cruthaithe: (2017)
  • On the spot: very local chromosomal rearrangements
    de réir: Helsmoortel, Céline, et al.
    Foilsithe / Cruthaithe: (2012)
  • Genomic Patterns of De Novo Mutation in Simplex Autism
    de réir: Tychele N. Turner, et al.
    Foilsithe / Cruthaithe: (2017)

Roghanna cuardaigh

  • Stair cuardach
  • Cuardach Casta

Aimsigh tuilleadh

  • Brabhsáil an chatalóg
  • Brabhsáil in ord aibítre
  • Míreanna nua

Cabhair uait?

  • Leideanna cuardaigh
  • Cuir ceist ar leabharlannaí
  • CCanna

Our networks:

  • Facebook Instagram Linkedin Youtube Spotify Tiktok

Developed by

Logo de acervos digitais