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Melanoma Research
|
June 1, 1995
CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families
N A Gruis, L A Sandkuijl, P A van der Velden, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
December 1, 1992
Lipoprotein profile of a Greenland Inuit population. Influence of anthropometric variables, Apo E and A4 polymorphism, and lifestyle
P de Knijff, L G Johansen, M Rosseneu, et al.
Gene
|
August 26, 1998
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates
P K Grewal, L C Todd, S van der Maarel, et al.
Atherosclerosis
|
October 1, 1991
Apolipoprotein E polymorphism affects plasma levels of lipoprotein(a)
P de Knijff, A Kaptein, D Boomsma, et al.
Human Molecular Genetics
|
October 1, 1993
Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11
T J Wright, C Wijmenga, L N Clark, et al.
Progress in Clinical and Biological Research
|
January 1, 1985
Urinary pepsinogen I: A multigene family?
J C Pronk, R R Frants, G Pals, et al.
Nucleic Acids Research
|
May 25, 1990
An additional MspI RFLP at the human hepatic lipase (HL) gene locus
R van Eyk, L Chan, B Top, et al.
Muscle & Nerve. Supplement
|
April 12, 2013
Facioscapulohumeral muscular dystrophy in the Dutch population
G W Padberg, R R Frants, O F Brouwer, et al.
Acta Ophthalmologica
|
August 1, 1983
Granular corneal dystrophy with late manifestation
H Forsius, A W Eriksson, J Kărnă, et al.
Biochemical and Biophysical Research Communications
|
August 15, 1991
Detection of allele-specific transcripts by the polymerase chain reaction (AST-PCR)
B Top, N van den Boorn, A van der Zee, et al.
Page
of 29
Search research articles
Search
Showing results (71-80 of 282) with videos related to
Sort By:
Page
of 29
Melanoma Research
|
June 1, 1995
CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families
N A Gruis, L A Sandkuijl, P A van der Velden, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
December 1, 1992
Lipoprotein profile of a Greenland Inuit population. Influence of anthropometric variables, Apo E and A4 polymorphism, and lifestyle
P de Knijff, L G Johansen, M Rosseneu, et al.
Gene
|
August 26, 1998
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates
P K Grewal, L C Todd, S van der Maarel, et al.
Atherosclerosis
|
October 1, 1991
Apolipoprotein E polymorphism affects plasma levels of lipoprotein(a)
P de Knijff, A Kaptein, D Boomsma, et al.
Human Molecular Genetics
|
October 1, 1993
Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11
T J Wright, C Wijmenga, L N Clark, et al.
Progress in Clinical and Biological Research
|
January 1, 1985
Urinary pepsinogen I: A multigene family?
J C Pronk, R R Frants, G Pals, et al.
Nucleic Acids Research
|
May 25, 1990
An additional MspI RFLP at the human hepatic lipase (HL) gene locus
R van Eyk, L Chan, B Top, et al.
Muscle & Nerve. Supplement
|
April 12, 2013
Facioscapulohumeral muscular dystrophy in the Dutch population
G W Padberg, R R Frants, O F Brouwer, et al.
Acta Ophthalmologica
|
August 1, 1983
Granular corneal dystrophy with late manifestation
H Forsius, A W Eriksson, J Kărnă, et al.
Biochemical and Biophysical Research Communications
|
August 15, 1991
Detection of allele-specific transcripts by the polymerase chain reaction (AST-PCR)
B Top, N van den Boorn, A van der Zee, et al.
Page
of 29