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P L Pearson

Showing results (161-170 of 211) with videos related to

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Nature|October 10, 1985
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16S T Reeders, M H Breuning, K E Davies, et al.
Human Genetics|November 1, 1986
Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophyM H Hofker, A A Bergen, M I Skraastad, et al.
Journal of Medical Genetics|September 1, 1989
Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutationsE Bakker, H Veenema, J T Den Dunnen, et al.
American Journal of Human Genetics|October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomesM H Hofker, M I Skraastad, A A Bergen, et al.
Molecular Reproduction and Development|June 11, 2005
Numerical chromosomal abnormalities in equine embryos produced in vivo and in vitroB P B Rambags, P J Krijtenburg, H F van Drie, et al.
Human Genetics|January 1, 1984
Localization of the polymorphic human calcitonin gene on chromosome 11J W Höppener, P H Steenbergh, J Zandberg, et al.
Neuromuscular Disorders : NMD|August 1, 2008
Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strengthC E Ambrósio, M C Valadares, E Zucconi, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|March 22, 2005
Studying the biological and technical sources of variation in telomere length of individual chromosomesE S D de Pauw, H Roelofs, A Zwinderman, et al.
Prenatal Diagnosis|July 1, 1988
First trimester prenatal diagnosis of haemophilia A: two years' experienceA H Bröcker-Vriends, E Briët, H H Kanhai, et al.
Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.
Pageof 22

Showing results (161-170 of 211) with videos related to

Sort By:
Pageof 22
Nature|October 10, 1985
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16S T Reeders, M H Breuning, K E Davies, et al.
Human Genetics|November 1, 1986
Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophyM H Hofker, A A Bergen, M I Skraastad, et al.
Journal of Medical Genetics|September 1, 1989
Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutationsE Bakker, H Veenema, J T Den Dunnen, et al.
American Journal of Human Genetics|October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomesM H Hofker, M I Skraastad, A A Bergen, et al.
Molecular Reproduction and Development|June 11, 2005
Numerical chromosomal abnormalities in equine embryos produced in vivo and in vitroB P B Rambags, P J Krijtenburg, H F van Drie, et al.
Human Genetics|January 1, 1984
Localization of the polymorphic human calcitonin gene on chromosome 11J W Höppener, P H Steenbergh, J Zandberg, et al.
Neuromuscular Disorders : NMD|August 1, 2008
Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strengthC E Ambrósio, M C Valadares, E Zucconi, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|March 22, 2005
Studying the biological and technical sources of variation in telomere length of individual chromosomesE S D de Pauw, H Roelofs, A Zwinderman, et al.
Prenatal Diagnosis|July 1, 1988
First trimester prenatal diagnosis of haemophilia A: two years' experienceA H Bröcker-Vriends, E Briët, H H Kanhai, et al.
Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.
Pageof 22