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P L Pearson

Showing results (101-110 of 211) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|April 7, 1990
[Procedure and initial results of presymptomatic DNA studies in Huntington's chorea]R A Roos, M Vegter-van der Vlis, A Tibben, et al.
Cancer Genetics and Cytogenetics|November 24, 1999
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.
Journal of Medical Genetics|July 1, 1987
The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27H Veenema, N J Carpenter, E Bakker, et al.
Birth Defects Original Article Series|January 1, 1976
Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybridsP Meera Khan, P L Pearson, L L Wijnen, et al.
Lancet (London, England)|November 19, 1983
Localisation of gene for Becker muscular dystrophyH M Kingston, P S Harper, P L Pearson, et al.
Nature|October 15, 1987
Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gelsJ T den Dunnen, E Bakker, E G Breteler, et al.
Clinical Genetics|June 1, 1988
The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986H Veenema, G C Beverstock, T de Koning, et al.
Nucleic Acids Research|November 11, 1987
Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studiesE Bakker, M I Skraastad, Y M Fisser-Groen, et al.
Human Genetics|July 1, 1987
Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGPM H Breuning, K Madan, M Verjaal, et al.
Human Genetics|January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophyD E Wilcox, N A Affara, J R Yates, et al.
Pageof 22

Showing results (101-110 of 211) with videos related to

Sort By:
Pageof 22
Nederlands Tijdschrift Voor Geneeskunde|April 7, 1990
[Procedure and initial results of presymptomatic DNA studies in Huntington's chorea]R A Roos, M Vegter-van der Vlis, A Tibben, et al.
Cancer Genetics and Cytogenetics|November 24, 1999
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.
Journal of Medical Genetics|July 1, 1987
The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27H Veenema, N J Carpenter, E Bakker, et al.
Birth Defects Original Article Series|January 1, 1976
Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybridsP Meera Khan, P L Pearson, L L Wijnen, et al.
Lancet (London, England)|November 19, 1983
Localisation of gene for Becker muscular dystrophyH M Kingston, P S Harper, P L Pearson, et al.
Nature|October 15, 1987
Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gelsJ T den Dunnen, E Bakker, E G Breteler, et al.
Clinical Genetics|June 1, 1988
The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986H Veenema, G C Beverstock, T de Koning, et al.
Nucleic Acids Research|November 11, 1987
Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studiesE Bakker, M I Skraastad, Y M Fisser-Groen, et al.
Human Genetics|July 1, 1987
Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGPM H Breuning, K Madan, M Verjaal, et al.
Human Genetics|January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophyD E Wilcox, N A Affara, J R Yates, et al.
Pageof 22