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Human Molecular Genetics
|
April 1, 1993
A simple and rapid PCR based method for AGU(Fin) determination
O Nilssen, O K Tollersrud, O Borud, et al.
American Journal of Medical Genetics
|
March 7, 2000
Jervell and Lange-Nielsen syndrome: a Norwegian perspective
L Tranebjaerg, J Bathen, J Tyson, et al.
European Journal of Pediatrics
|
October 3, 2000
Immunodeficiency in alpha-mannosidosis: a matched case-control study on immunoglobulins, complement factors, receptor density, phagocytosis and intracellular killing in leucocytes
D Malm, D S Halvorsen, L Tranebjaerg, et al.
Human Genetics
|
May 1, 1997
The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletions
J Nardmann, L Tranebjaerg, B Horsthemke, et al.
American Journal of Medical Genetics
|
July 12, 1996
Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndrome
K H Orstavik, R E Orstavik, K Eiklid, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 20, 1995
[Alpha-mannosidosis]
D Malm, O K Tollersrud, L Tranebjaerg, et al.
Annales De Genetique
|
January 1, 1984
Clinical and cytogenetic studies in a large (4;8) translocation family with pre- and postnatal Wolf syndrome
L Tranebjaerg, A Petersen, K Hove, et al.
Hereditas
|
January 1, 1989
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22
K Arheden, U Tantravahi, N Tommerup, et al.
Clinical Genetics
|
August 1, 1987
Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23)
L Tranebjaerg, U B Baekmark, M Dyhr-Nielsen, et al.
European Journal of Human Genetics : EJHG
|
February 13, 2002
Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia
C Sun, L Tranebjaerg, T Torbergsen, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 107) with videos related to
Sort By:
Page
of 11
Human Molecular Genetics
|
April 1, 1993
A simple and rapid PCR based method for AGU(Fin) determination
O Nilssen, O K Tollersrud, O Borud, et al.
American Journal of Medical Genetics
|
March 7, 2000
Jervell and Lange-Nielsen syndrome: a Norwegian perspective
L Tranebjaerg, J Bathen, J Tyson, et al.
European Journal of Pediatrics
|
October 3, 2000
Immunodeficiency in alpha-mannosidosis: a matched case-control study on immunoglobulins, complement factors, receptor density, phagocytosis and intracellular killing in leucocytes
D Malm, D S Halvorsen, L Tranebjaerg, et al.
Human Genetics
|
May 1, 1997
The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletions
J Nardmann, L Tranebjaerg, B Horsthemke, et al.
American Journal of Medical Genetics
|
July 12, 1996
Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndrome
K H Orstavik, R E Orstavik, K Eiklid, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 20, 1995
[Alpha-mannosidosis]
D Malm, O K Tollersrud, L Tranebjaerg, et al.
Annales De Genetique
|
January 1, 1984
Clinical and cytogenetic studies in a large (4;8) translocation family with pre- and postnatal Wolf syndrome
L Tranebjaerg, A Petersen, K Hove, et al.
Hereditas
|
January 1, 1989
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22
K Arheden, U Tantravahi, N Tommerup, et al.
Clinical Genetics
|
August 1, 1987
Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23)
L Tranebjaerg, U B Baekmark, M Dyhr-Nielsen, et al.
European Journal of Human Genetics : EJHG
|
February 13, 2002
Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia
C Sun, L Tranebjaerg, T Torbergsen, et al.
Page
of 11