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S Blaser

Showing results (61-70 of 85) with videos related to

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AJNR. American Journal of Neuroradiology|September 1, 1989
Gd-DTPA enhancement of posterior epidural scar: an experimental modelJ S Ross, S Blaser, T J Masaryk, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 15, 2008
Rhombencephalosynapsis: prenatal imaging and autopsy findingsF McAuliffe, D Chitayat, W Halliday, et al.
Optics Express|March 26, 2014
Intermittent operation of QC-lasers for mid-IR spectroscopy with low heat dissipation: tuning characteristics and driving electronicsM Fischer, B Tuzson, A Hugi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 11, 2010
Fetal forehead hemangiopericytoma: prenatal diagnosis and postnatal outcomeH Y B Chung, L Chu, C Forrest, et al.
American Journal of Medical Genetics|March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotypeD Chitayat, A Toi, R Babul, et al.
Neurosurgery|May 1, 1993
Primary leptomeningeal melanoma: an unusually aggressive tumor in childhoodD Allcutt, S Michowiz, S Weitzman, et al.
AJNR. American Journal of Neuroradiology|December 6, 2001
Optic pathway glioma: correlation of imaging findings with the presence of neurofibromatosisL Kornreich, S Blaser, M Schwarz, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutationC P Barnett, R Mendoza-Londono, S Blaser, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
Clinical Genetics|October 9, 2016
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactylyK D Kernohan, A McBride, Y Xi, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
AJNR. American Journal of Neuroradiology|September 1, 1989
Gd-DTPA enhancement of posterior epidural scar: an experimental modelJ S Ross, S Blaser, T J Masaryk, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 15, 2008
Rhombencephalosynapsis: prenatal imaging and autopsy findingsF McAuliffe, D Chitayat, W Halliday, et al.
Optics Express|March 26, 2014
Intermittent operation of QC-lasers for mid-IR spectroscopy with low heat dissipation: tuning characteristics and driving electronicsM Fischer, B Tuzson, A Hugi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 11, 2010
Fetal forehead hemangiopericytoma: prenatal diagnosis and postnatal outcomeH Y B Chung, L Chu, C Forrest, et al.
American Journal of Medical Genetics|March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotypeD Chitayat, A Toi, R Babul, et al.
Neurosurgery|May 1, 1993
Primary leptomeningeal melanoma: an unusually aggressive tumor in childhoodD Allcutt, S Michowiz, S Weitzman, et al.
AJNR. American Journal of Neuroradiology|December 6, 2001
Optic pathway glioma: correlation of imaging findings with the presence of neurofibromatosisL Kornreich, S Blaser, M Schwarz, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutationC P Barnett, R Mendoza-Londono, S Blaser, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
Clinical Genetics|October 9, 2016
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactylyK D Kernohan, A McBride, Y Xi, et al.
Pageof 9