Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Genetic services in Norway

L Tranebjaerg1, A L Børresen-Dale, I L Hansteen

  • 1Department of Medical Genetics, Regionsykehuseti Tromsø, Norway.

European Journal of Human Genetics : EJHG
|January 1, 1997
PubMed
Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Nuclear CSPP1 expression defined subtypes of basal-like breast cancer.

British journal of cancer·2014
Same author

Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patients.

Advances in medical sciences·2013
Same author

SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations.

Clinical genetics·2013
Same author

Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome.

Clinical genetics·2012
Same author

Identification of genetic variation in 11 candidate genes of canine mammary tumour.

Veterinary and comparative oncology·2011
Same author

Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.

Clinical genetics·2011
Same journal

Parental and public views on genomic newborn screening: a systematic review.

European journal of human genetics : EJHG·2026
Same journal

Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network.

European journal of human genetics : EJHG·2026
Same journal

Characterisation of the SMN1/2 locus using a highly specific variant caller on whole-genome sequence data from 500,000 individuals.

European journal of human genetics : EJHG·2026
Same journal

When truncation is not loss of function: neo-tail architecture as a determinant of pathogenicity in NMD-escaping frameshift variants.

European journal of human genetics : EJHG·2026
Same journal

CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders.

European journal of human genetics : EJHG·2026
Same journal

Parent and professional experiences of a clinical trial of prenatal and postnatal stem cell therapy for severe osteogenesis imperfecta.

European journal of human genetics : EJHG·2026
See all related articles