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Research | 1 May 1997
The ability to cleave 28S ribosomal RNA during apoptosis is a cell-type dependent trait unrelated to DNA fragmentation
- gunnar.houge@gen.haukeland.no
Cell Death & Differentiation 4 , 289–293

Rights & permissionsfor article The ability to cleave 28S ribosomal RNA during apoptosis is a cell-type dependent trait unrelated to DNA fragmentation . Opens in a new window.
Reviews | 1 December 2017
Secretary Generals on recent ESHG presidents (2003–2015)
- A biopic of Gunnar Houge appears earlier in this issue...
- Helena Kääriäinen
- & Gunnar Houge
European Journal of Human Genetics 25 , S20–S22

Rights & permissionsfor article Secretary Generals on recent ESHG presidents (2003–2015) . Opens in a new window.
Research | 7 March 2007
Angioma serpiginosum with oesophageal papillomatosis is an X-linked dominant condition that maps to Xp11.3–Xq12
- gunnar.houge@helse-bergen.no
European Journal of Human Genetics 15 , 543–547

Rights & permissionsfor article Angioma serpiginosum with oesophageal papillomatosis is an X-linked dominant condition that maps to Xp11.3–Xq12 . Opens in a new window.
Research | 10 April 2013 | Open
Evidence for anticipation in Beckwith–Wiedemann syndrome
- gunnar.houge@helse-bergen.no
- Siren Berland
- , Mia Appelbäck
- , Ove Bruland
- , Jasmin Beygo
- , Karin Buiting
- , Deborah J G Mackay
- , I Karen Temple
- & Gunnar Houge
European Journal of Human Genetics 21 , 1344–1348

Rights & permissionsfor article Evidence for anticipation in Beckwith–Wiedemann syndrome . Opens in a new window.
Research | 27 October 2020 | Open
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction
- gunnar.houge@helse-bergen.no
- Lisa Lenaerts
- , Sara Reynhout
- , Iris Verbinnen
- , Frédéric Laumonnier
- , Annick Toutain
- , Frédérique Bonnet-Brilhault
- , Yana Hoorne
- , Shelagh Joss
- , Anna K. Chassevent
- , Constance Smith-Hicks
- , Bart Loeys
- , Pascal Joset
- , Katharina Steindl
- , Anita Rauch
- , Sarju G. Mehta
- , Wendy K. Chung
- , Koenraad Devriendt
- , Susan E. Holder
- , Tamison Jewett
- , Lauren M. Baldwin
- , William G. Wilson
- , Shelley Towner
- , Siddharth Srivastava
- , Hannah F. Johnson
- , Cornelia Daumer-Haas
- , Martina Baethmann
- , Anna Ruiz
- , Elisabeth Gabau
- , Vani Jain
- , Vinod Varghese
- , Ali Al-Beshri
- , Stephen Fulton
- , Oded Wechsberg
- , Naama Orenstein
- , Katrina Prescott
- , Anne-Marie Childs
- , Laurence Faivre
- , Sébastien Moutton
- , Jennifer A. Sullivan
- , Vandana Shashi
- , Suzanne M. Koudijs
- , Malou Heijligers
- , Emma Kivuva
- , Amy McTague
- , Alison Male
- , Yvette van Ierland
- , Barbara Plecko
- , Isabelle Maystadt
- , Rizwan Hamid
- , Vickie L. Hannig
- , Gunnar Houge
- & Veerle Janssens
Genetics in Medicine 23 , 352–362

Rights & permissionsfor article The broad phenotypic spectrum of <i>PPP2R1A</i>-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction . Opens in a new window.
Reviews | 1 December 2017
The inner life and structure of ESHG
- gunnar.houge@helse-bergen.no
- Gunnar Houge
- & Jerome del Picchia
European Journal of Human Genetics 25 , S16–S19

Rights & permissionsfor article The inner life and structure of ESHG . Opens in a new window.
Research | 20 December 2018
A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome
- gunnar.houge@helse-bergen.no
- Cecilie Bredrup
- , Tomasz Stokowy
- , Julie McGaughran
- , Samuel Lee
- , Dipak Sapkota
- , Ileana Cristea
- , Linda Xu
- , Kåre Steinar Tveit
- , Gunnar Høvding
- , Vidar Martin Steen
- , Eyvind Rødahl
- , Ove Bruland
- & Gunnar Houge
European Journal of Human Genetics 27 , 574–581

Rights & permissionsfor article A tyrosine kinase-activating variant Asn666Ser in <i>PDGFRB</i> causes a progeria-like condition in the severe end of Penttinen syndrome . Opens in a new window.
Correspondence | 1 April 2009
Reply to Happle
- gunnar.houge@helse-bergen.no
- Gunnar Houge
- & Raoul C M Hennekam
European Journal of Human Genetics 17 , 882–882

Rights & permissionsfor article Reply to Happle . Opens in a new window.
Correspondence | 14 May 2008
An Xp11.23 deletion containing PORCN may also cause angioma serpiginosum, a cosmetic skin disease associated with extreme skewing of X-inactivation
- gunnar.houge@helse-bergen.no
European Journal of Human Genetics 16 , 1027–1028

Rights & permissionsfor article An Xp11.23 deletion containing <i>PORCN</i> may also cause angioma serpiginosum, a cosmetic skin disease associated with extreme skewing of X-inactivation . Opens in a new window.
Correspondence | 18 May 2011
Fabry or not Fabry – a question of ascertainment
- gunnar.houge@helse-bergen.no
- Gunnar Houge
- , Camilla Tøndel
- , Øyvind Kaarbøe
- , Asle Hirth
- , Leif Bostad
- & Einar Svarstad
European Journal of Human Genetics 19 , 1111–1111

Rights & permissionsfor article Fabry or not Fabry – a question of ascertainment . Opens in a new window.

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