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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 20, 2002
[Screening for DiGeorge syndrome and other genetic diseases]
Gunnar Houge
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 8, 2015
[Where is the boundary between diagnostics and research?]
Gunnar Houge
European Journal of Human Genetics : EJHG
|
January 4, 2018
Secretary Generals on recent ESHG presidents (2003-2015)
Helena Kääriäinen, Gunnar Houge
Clinical Dysmorphology
|
August 24, 2010
Late-onset gain of skills and peculiar jugular pit in an 11-year-old girl with 5q14.3 microdeletion including MEF2C
Siren Berland, Gunnar Houge
American Journal of Human Genetics
|
January 7, 2014
Loss of PRDM16 is unlikely to cause cardiomyopathy in 1p36 deletion syndrome
Nicole de Leeuw, Gunnar Houge
European Journal of Human Genetics : EJHG
|
January 4, 2018
The inner life and structure of ESHG
Gunnar Houge, Jerome Del Picchia
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 18, 2003
[Diagnosis of cryptic chromosome aberrations]
Gro Oddveig Ness, Gunnar Houge
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
April 27, 2005
[Fabry disease--a diagnostic and therapeutic challenge]
Gunnar Houge, Alv Johan Skarbøvik
Autism Research : Official Journal of the International Society for Autism Research
|
May 31, 2023
Locus conversions are rare in the LRFN5 locus
Jacob Sampson, , Gunnar Houge, et al.
BMC Medical Genetics
|
May 19, 2009
Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: a result of failed tetraploidy correction?
Gunnar Houge, Helle Lybaek, Sasha Gulati
Page
of 13
Search research articles
Search
Showing results (1-10 of 125) with videos related to
Sort By:
Page
of 13
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 20, 2002
[Screening for DiGeorge syndrome and other genetic diseases]
Gunnar Houge
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 8, 2015
[Where is the boundary between diagnostics and research?]
Gunnar Houge
European Journal of Human Genetics : EJHG
|
January 4, 2018
Secretary Generals on recent ESHG presidents (2003-2015)
Helena Kääriäinen, Gunnar Houge
Clinical Dysmorphology
|
August 24, 2010
Late-onset gain of skills and peculiar jugular pit in an 11-year-old girl with 5q14.3 microdeletion including MEF2C
Siren Berland, Gunnar Houge
American Journal of Human Genetics
|
January 7, 2014
Loss of PRDM16 is unlikely to cause cardiomyopathy in 1p36 deletion syndrome
Nicole de Leeuw, Gunnar Houge
European Journal of Human Genetics : EJHG
|
January 4, 2018
The inner life and structure of ESHG
Gunnar Houge, Jerome Del Picchia
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 18, 2003
[Diagnosis of cryptic chromosome aberrations]
Gro Oddveig Ness, Gunnar Houge
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
April 27, 2005
[Fabry disease--a diagnostic and therapeutic challenge]
Gunnar Houge, Alv Johan Skarbøvik
Autism Research : Official Journal of the International Society for Autism Research
|
May 31, 2023
Locus conversions are rare in the LRFN5 locus
Jacob Sampson, , Gunnar Houge, et al.
BMC Medical Genetics
|
May 19, 2009
Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: a result of failed tetraploidy correction?
Gunnar Houge, Helle Lybaek, Sasha Gulati
Page
of 13