C Klingenberg|K Fossen|L Tranebjaerg - JoVE Visualize

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 20, 1991

[Opiate-related deaths among drug addicts. Autopsy findings, circumstances and forensic toxicologic analyses regarding deaths]O M Filseth, K Fossen, V B Halvorsen, et al.

Tissue Antigens|April 26, 2002

HLA profile of three ethnic groups living in the North-Western region of RussiaI Evseeva, A Spurkland, E Thorsby, et al.

American Journal of Medical Genetics|May 1, 1988

Linkage analysis suggests at least two loci for X-linked non-specific mental retardationB Arveiler, Y Alembik, A Hanauer, et al.

Ophthalmic Genetics|January 3, 2001

Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.

Journal of Medical Genetics|April 1, 1995

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22L Tranebjaerg, C Schwartz, H Eriksen, et al.

Human Molecular Genetics|May 1, 1997

alpha-Mannosidosis: functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblingsO Nilssen, T Berg, H M Riise, et al.

American Journal of Human Genetics|January 1, 1991

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndromeM B Petersen, A A Schinzel, F Binkert, et al.

Advances in Medical Sciences|November 14, 2013

Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patientsR Teek, K Kruustük, R Žordania, et al.

Clinical Genetics|July 1, 1993

Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patientsK Eiklid, L Tranebjaerg, H G Eiken, et al.

Allergy|April 6, 2017

Staphylococcus aureus enterotoxin sensitization is associated with allergic poly-sensitization and allergic multimorbidity in adolescentsM Sørensen, C Klingenberg, M Wickman, et al.

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Showing results (61-70 of 103) with videos related to

Sort By:

Pageof 11

Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 20, 1991

[Opiate-related deaths among drug addicts. Autopsy findings, circumstances and forensic toxicologic analyses regarding deaths]O M Filseth, K Fossen, V B Halvorsen, et al.

Tissue Antigens|April 26, 2002

HLA profile of three ethnic groups living in the North-Western region of RussiaI Evseeva, A Spurkland, E Thorsby, et al.

American Journal of Medical Genetics|May 1, 1988

Linkage analysis suggests at least two loci for X-linked non-specific mental retardationB Arveiler, Y Alembik, A Hanauer, et al.

Ophthalmic Genetics|January 3, 2001

Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.

Journal of Medical Genetics|April 1, 1995

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22L Tranebjaerg, C Schwartz, H Eriksen, et al.

Human Molecular Genetics|May 1, 1997

alpha-Mannosidosis: functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblingsO Nilssen, T Berg, H M Riise, et al.

American Journal of Human Genetics|January 1, 1991

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndromeM B Petersen, A A Schinzel, F Binkert, et al.

Advances in Medical Sciences|November 14, 2013

Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patientsR Teek, K Kruustük, R Žordania, et al.

Clinical Genetics|July 1, 1993

Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patientsK Eiklid, L Tranebjaerg, H G Eiken, et al.

Allergy|April 6, 2017

Staphylococcus aureus enterotoxin sensitization is associated with allergic poly-sensitization and allergic multimorbidity in adolescentsM Sørensen, C Klingenberg, M Wickman, et al.

Pageof 11