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P L Pearson

Showing results (171-180 of 211) with videos related to

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Human Genetics|November 1, 1986
A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locusH Scheffer, D van der Lelie, G H Aanstoot, et al.
Clinical Genetics|January 23, 2009
A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21K Lezirovitz, M C C Braga, R S Thiele-Aguiar, et al.
American Journal of Human Genetics|April 1, 1989
Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 regionM I Skraastad, E Bakker, L F de Lange, et al.
Human Reproduction (Oxford, England)|August 31, 2001
The role of genetic factors in age at natural menopauseJ P de Bruin, H Bovenhuis, P A van Noord, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 15, 1985
[Search for the carrier state of hemophilia B using restriction fragment length polymorphism]E Briët, A Bröcker-Vriends, R Quadt, et al.
American Journal of Human Genetics|April 1, 1987
Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardationM H Hofker, A A Bergen, M I Skraastad, et al.
British Medical Journal (Clinical Research Ed.)|March 29, 1986
Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16S T Reeders, M H Breuning, G Corney, et al.
American Journal of Medical Genetics|May 1, 1991
Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markersM I Skraastad, A Verwest, E Bakker, et al.
American Journal of Human Genetics|October 1, 1988
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.
Thrombosis and Haemostasis|April 7, 1987
Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphismsA H Bröcker-Vriends, E Briët, R Quadt, et al.
Pageof 22

Showing results (171-180 of 211) with videos related to

Sort By:
Pageof 22
Human Genetics|November 1, 1986
A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locusH Scheffer, D van der Lelie, G H Aanstoot, et al.
Clinical Genetics|January 23, 2009
A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21K Lezirovitz, M C C Braga, R S Thiele-Aguiar, et al.
American Journal of Human Genetics|April 1, 1989
Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 regionM I Skraastad, E Bakker, L F de Lange, et al.
Human Reproduction (Oxford, England)|August 31, 2001
The role of genetic factors in age at natural menopauseJ P de Bruin, H Bovenhuis, P A van Noord, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 15, 1985
[Search for the carrier state of hemophilia B using restriction fragment length polymorphism]E Briët, A Bröcker-Vriends, R Quadt, et al.
American Journal of Human Genetics|April 1, 1987
Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardationM H Hofker, A A Bergen, M I Skraastad, et al.
British Medical Journal (Clinical Research Ed.)|March 29, 1986
Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16S T Reeders, M H Breuning, G Corney, et al.
American Journal of Medical Genetics|May 1, 1991
Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markersM I Skraastad, A Verwest, E Bakker, et al.
American Journal of Human Genetics|October 1, 1988
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.
Thrombosis and Haemostasis|April 7, 1987
Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphismsA H Bröcker-Vriends, E Briët, R Quadt, et al.
Pageof 22