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L Mandel

Showing results (231-240 of 451) with videos related to

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European Journal of Human Genetics : EJHG|January 15, 1999
Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)C Broccardo, N Troffer-Charlier, S Savary, et al.
The American Journal of Medicine|February 1, 1989
Occult polymicrobial endocarditis with Haemophilus parainfluenzae in intravenous drug abusersB Raucher, J Dobkin, L Mandel, et al.
Violence and Victims|March 10, 2015
The occurrence of female-to-male partner violence among male intimate partner violence offenders mandated to treatment: a brief research reportCory A Crane, Samuel W Hawes, Dolores L Mandel, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasiaM C Vincent, V Biancalana, D Ginisty, et al.
Biochimica Et Biophysica Acta|June 24, 1983
Similarity of genetic distance determined from DNA thermal denaturation profiles to standard estimates of bacteriophage relatednessA T Ansevin, D L Vizard, M L Mandel, et al.
Nature Communications|June 23, 2022
Single molecule demonstration of Debye-Stokes-Einstein breakdown in polystyrene near the glass transition temperatureNicole L Mandel, Soohyun Lee, Kimyung Kim, et al.
Acta Universitatis Palackianae Olomucensis Facultatis Medicae|January 1, 1990
Postirradiation changes in small intestine mucosa of piglets selectively decontaminated by peroral antibioticsJ Pospísilová, V Kamarád, V Svoboda, et al.
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.
Lancet (London, England)|April 13, 1985
Polymorphic DNA markers in prenatal diagnosis of fragile X syndromeI Oberlé, J L Mandel, J Boué, et al.
Science (New York, N.Y.)|October 2, 1992
Genome analysis and the human X chromosomeJ L Mandel, A P Monaco, D L Nelson, et al.
Pageof 46

Showing results (231-240 of 451) with videos related to

Sort By:
Pageof 46
European Journal of Human Genetics : EJHG|January 15, 1999
Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)C Broccardo, N Troffer-Charlier, S Savary, et al.
The American Journal of Medicine|February 1, 1989
Occult polymicrobial endocarditis with Haemophilus parainfluenzae in intravenous drug abusersB Raucher, J Dobkin, L Mandel, et al.
Violence and Victims|March 10, 2015
The occurrence of female-to-male partner violence among male intimate partner violence offenders mandated to treatment: a brief research reportCory A Crane, Samuel W Hawes, Dolores L Mandel, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasiaM C Vincent, V Biancalana, D Ginisty, et al.
Biochimica Et Biophysica Acta|June 24, 1983
Similarity of genetic distance determined from DNA thermal denaturation profiles to standard estimates of bacteriophage relatednessA T Ansevin, D L Vizard, M L Mandel, et al.
Nature Communications|June 23, 2022
Single molecule demonstration of Debye-Stokes-Einstein breakdown in polystyrene near the glass transition temperatureNicole L Mandel, Soohyun Lee, Kimyung Kim, et al.
Acta Universitatis Palackianae Olomucensis Facultatis Medicae|January 1, 1990
Postirradiation changes in small intestine mucosa of piglets selectively decontaminated by peroral antibioticsJ Pospísilová, V Kamarád, V Svoboda, et al.
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.
Lancet (London, England)|April 13, 1985
Polymorphic DNA markers in prenatal diagnosis of fragile X syndromeI Oberlé, J L Mandel, J Boué, et al.
Science (New York, N.Y.)|October 2, 1992
Genome analysis and the human X chromosomeJ L Mandel, A P Monaco, D L Nelson, et al.
Pageof 46