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Scandinavian Journal of Clinical and Laboratory Investigation
|
November 1, 1991
Evaluation of DNA-based diagnosis for haemophilia A
C Wadelius, M Blombäck, P Goonewardena, et al.
Human Mutation
|
April 24, 2001
Identification of four novel polymorphisms in the calcitonin/alpha-CGRP (CALCA) gene and an investigation of their possible associations with Parkinson disease, schizophrenia, and manic depression
S Buervenich, F Xiang, O Sydow, et al.
The Journal of Biological Chemistry
|
April 5, 2000
Independent regulation of the myotonic dystrophy 1 locus genes postnatally and during adult skeletal muscle regeneration
M Eriksson, T Ansved, L Edstrom, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
November 1, 1993
Genetic carrier detection in Norwegian families with acute intermittent porphyria
E Sagen, A Laegreid, M Anvret, et al.
Clinical Genetics
|
June 1, 1988
A linkage study of the locus for X-linked Charcot-Marie-Tooth disease
P Goonewardena, J Welihinda, M Anvret, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
May 7, 2002
APOE genotypes and disease severity in multiple sclerosis
T Masterman, Z Zhang, D Hellgren, et al.
Clinical Genetics
|
December 1, 1991
Genetic mapping of loci for X-linked retinitis pigmentosa
N Dahl, M Sundvall, U Pettersson, et al.
Pediatric Research
|
November 14, 1997
Increased leptin messenger RNA and serum leptin levels in children with Prader-Willi syndrome and nonsyndromal obesity
A C Lindgren, C Marcus, C Skwirut, et al.
Human Genetics
|
August 1, 1988
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria
J S Lee, M Anvret, J Lindsten, et al.
American Journal of Human Genetics
|
May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes
A Reis, B Dittrich, V Greger, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
Scandinavian Journal of Clinical and Laboratory Investigation
|
November 1, 1991
Evaluation of DNA-based diagnosis for haemophilia A
C Wadelius, M Blombäck, P Goonewardena, et al.
Human Mutation
|
April 24, 2001
Identification of four novel polymorphisms in the calcitonin/alpha-CGRP (CALCA) gene and an investigation of their possible associations with Parkinson disease, schizophrenia, and manic depression
S Buervenich, F Xiang, O Sydow, et al.
The Journal of Biological Chemistry
|
April 5, 2000
Independent regulation of the myotonic dystrophy 1 locus genes postnatally and during adult skeletal muscle regeneration
M Eriksson, T Ansved, L Edstrom, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
November 1, 1993
Genetic carrier detection in Norwegian families with acute intermittent porphyria
E Sagen, A Laegreid, M Anvret, et al.
Clinical Genetics
|
June 1, 1988
A linkage study of the locus for X-linked Charcot-Marie-Tooth disease
P Goonewardena, J Welihinda, M Anvret, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
May 7, 2002
APOE genotypes and disease severity in multiple sclerosis
T Masterman, Z Zhang, D Hellgren, et al.
Clinical Genetics
|
December 1, 1991
Genetic mapping of loci for X-linked retinitis pigmentosa
N Dahl, M Sundvall, U Pettersson, et al.
Pediatric Research
|
November 14, 1997
Increased leptin messenger RNA and serum leptin levels in children with Prader-Willi syndrome and nonsyndromal obesity
A C Lindgren, C Marcus, C Skwirut, et al.
Human Genetics
|
August 1, 1988
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria
J S Lee, M Anvret, J Lindsten, et al.
American Journal of Human Genetics
|
May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes
A Reis, B Dittrich, V Greger, et al.
Page
of 14