Human molecular genetics, 2013-04, Vol.22 (8), p.1654-1662
- Twigg, Stephen R.F.
- Babbs, Christian
- van den Elzen, Marijke E.P.
- Goriely, Anne
- Taylor, Stephen
- McGowan, Simon J.
- Giannoulatou, Eleni
- Lonie, Lorne
- Ragoussis, Jiannis
- Akha, Elham Sadighi
- Knight, Samantha J.L.
- Zechi-Ceide, Roseli M.
- Hoogeboom, Jeannette A.M.
- Pober, Barbara R.
- Toriello, Helga V.
- Wall, Steven A.
- Rita Passos-Bueno, M.
- Brunner, Han G.
- Mathijssen, Irene M.J.
- Wilkie, Andrew O.M.
2013
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- Autor(en) / Beteiligte
- Twigg, Stephen R.F.
- Babbs, Christian
- van den Elzen, Marijke E.P.
- Goriely, Anne
- Taylor, Stephen
- McGowan, Simon J.
- Giannoulatou, Eleni
- Lonie, Lorne
- Ragoussis, Jiannis
- Akha, Elham Sadighi
- Knight, Samantha J.L.
- Zechi-Ceide, Roseli M.
- Hoogeboom, Jeannette A.M.
- Pober, Barbara R.
- Toriello, Helga V.
- Wall, Steven A.
- Rita Passos-Bueno, M.
- Brunner, Han G.
- Mathijssen, Irene M.J.
- Wilkie, Andrew O.M.
- Titel
- Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes
- Ist Teil von
- Human molecular genetics, 2013-04, Vol.22 (8), p.1654-1662
- Erscheinungsjahr
- 2013
- Quelle
- Oxford Journals 2020 Medicine
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0964-6906eISSN: 1460-2083DOI: 10.1093/hmg/ddt015Titel-ID: cdi_crossref_primary_10_1093_hmg_ddt015
- Format
- –