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P L Pearson

Showing results (141-150 of 211) with videos related to

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Cancer Genetics and Cytogenetics|March 24, 1999
Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell linesJ Kuipers, J W Vaandrager, D O Weghuis, et al.
Progress in Clinical and Biological Research|January 1, 1989
Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysisE Bakker, E J Bonten, J T den Dunnen, et al.
Human Genetics|December 1, 1988
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursM Mannens, R M Slater, C Heyting, et al.
Human Genetics|January 1, 1985
The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24F Baas, H Bikker, A Geurts van Kessel, et al.
Human Genetics|August 1, 1986
Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridizationJ E Landegent, N Jansen in de Wal, Y M Fisser-Groen, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving fieldE Bakker, E J Bonten, H Veenema, et al.
Human Reproduction (Oxford, England)|April 1, 1997
Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoaP A In't Veld, F J Broekmans, H F de France, et al.
Journal of Medical Genetics|March 1, 1974
A kindred with familial cold urticaria: linkage analysisH M Doeglas, L F Bernini, G R Fraser, et al.
Molecular Psychiatry|August 11, 2004
Neuregulin 1: genetic support for schizophrenia subtypesS C Bakker, M L C Hoogendoorn, J-P Selten, et al.
Cancer Research|October 15, 1988
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probesP Devilee, R F Thierry, T Kievits, et al.
Pageof 22

Showing results (141-150 of 211) with videos related to

Sort By:
Pageof 22
Cancer Genetics and Cytogenetics|March 24, 1999
Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell linesJ Kuipers, J W Vaandrager, D O Weghuis, et al.
Progress in Clinical and Biological Research|January 1, 1989
Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysisE Bakker, E J Bonten, J T den Dunnen, et al.
Human Genetics|December 1, 1988
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursM Mannens, R M Slater, C Heyting, et al.
Human Genetics|January 1, 1985
The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24F Baas, H Bikker, A Geurts van Kessel, et al.
Human Genetics|August 1, 1986
Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridizationJ E Landegent, N Jansen in de Wal, Y M Fisser-Groen, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving fieldE Bakker, E J Bonten, H Veenema, et al.
Human Reproduction (Oxford, England)|April 1, 1997
Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoaP A In't Veld, F J Broekmans, H F de France, et al.
Journal of Medical Genetics|March 1, 1974
A kindred with familial cold urticaria: linkage analysisH M Doeglas, L F Bernini, G R Fraser, et al.
Molecular Psychiatry|August 11, 2004
Neuregulin 1: genetic support for schizophrenia subtypesS C Bakker, M L C Hoogendoorn, J-P Selten, et al.
Cancer Research|October 15, 1988
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probesP Devilee, R F Thierry, T Kievits, et al.
Pageof 22