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M Riegel

Showing results (21-30 of 48) with videos related to

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American Journal of Medical Genetics|October 6, 1999
Short stature, myopia, severe developmental delay, and peculiar facial appearance in two brothers: a new syndrome?S Achermann, R Largo, D Kotzot, et al.
Epilepsy Research|October 24, 2001
Epilepsy and trisomy 19q--different seizure patterns in a brother and a sisterT Dorn, M Riegel, A Schinzel, et al.
Journal of Ocular Pharmacology|January 1, 1994
Intraocular diclofenac and flurbiprofen concentrations in human aqueous humor following topical applicationP P Ellis, D S Pfoff, D C Bloedow, et al.
Veterinary Clinical Pathology|September 3, 2008
What is your diagnosis? Muculent pleural effusion from a dogCasey M Riegel, Steven L Stockham, Kristin M Patton, et al.
Scientific Reports|March 2, 2018
Cognitive control over memory - individual differences in memory performance for emotional and neutral materialM Wierzba, M Riegel, M Wypych, et al.
European Journal of Pediatrics|February 24, 2001
Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial (Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2S Fokstuen, K Vrticka, M Riegel, et al.
European Journal of Medical Genetics|August 2, 2005
Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21M Riegel, P Hargreaves, A Baumer, et al.
Human Genetics|November 10, 2001
Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromesM Riegel, A Baumer, M Jamar, et al.
Molecular Endocrinology (Baltimore, Md.)|December 25, 2004
Novel association of Vav2 and Nek3 modulates signaling through the human prolactin receptorSommer L Miller, Jamie E DeMaria, David O Freier, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Assignment of the gene encoding the neuronal multidomain serine protease neurotrypsin (PRSS12) to human chromosome band 4q25-->q26 by in situ hybridizationS V Kozlov, M Riegel, J Kinter, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|October 6, 1999
Short stature, myopia, severe developmental delay, and peculiar facial appearance in two brothers: a new syndrome?S Achermann, R Largo, D Kotzot, et al.
Epilepsy Research|October 24, 2001
Epilepsy and trisomy 19q--different seizure patterns in a brother and a sisterT Dorn, M Riegel, A Schinzel, et al.
Journal of Ocular Pharmacology|January 1, 1994
Intraocular diclofenac and flurbiprofen concentrations in human aqueous humor following topical applicationP P Ellis, D S Pfoff, D C Bloedow, et al.
Veterinary Clinical Pathology|September 3, 2008
What is your diagnosis? Muculent pleural effusion from a dogCasey M Riegel, Steven L Stockham, Kristin M Patton, et al.
Scientific Reports|March 2, 2018
Cognitive control over memory - individual differences in memory performance for emotional and neutral materialM Wierzba, M Riegel, M Wypych, et al.
European Journal of Pediatrics|February 24, 2001
Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial (Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2S Fokstuen, K Vrticka, M Riegel, et al.
European Journal of Medical Genetics|August 2, 2005
Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21M Riegel, P Hargreaves, A Baumer, et al.
Human Genetics|November 10, 2001
Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromesM Riegel, A Baumer, M Jamar, et al.
Molecular Endocrinology (Baltimore, Md.)|December 25, 2004
Novel association of Vav2 and Nek3 modulates signaling through the human prolactin receptorSommer L Miller, Jamie E DeMaria, David O Freier, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Assignment of the gene encoding the neuronal multidomain serine protease neurotrypsin (PRSS12) to human chromosome band 4q25-->q26 by in situ hybridizationS V Kozlov, M Riegel, J Kinter, et al.
Pageof 5