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S Fallet

Showing results (1-10 of 10) with videos related to

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Pediatric Cardiology|April 8, 2000
Patients' age at time of testing for chromosome 22q11 microdeletions: missed opportunities for genetic counselingY Liu, S Fallet, R Koppel
American Journal of Medical Genetics|August 23, 1996
Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literatureR Koppel, S Friedman, S Fallet
American Journal of Medical Genetics|January 23, 1999
Mosaicism with a normal cell line and an unbalanced structural rearrangementA L Zaslav, S Fallet, D Blumenthal, et al.
Prenatal Diagnosis|March 1, 1993
Prenatal detection of monosomy 21 mosaicismA Ghidini, S Fallet, J Robinowitz, et al.
Clinical Genetics|July 3, 1998
Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literatureA L Zaslav, S Fallet, S Brown, et al.
Nature Genetics|January 1, 1996
A two-hit model for developmental defects in Gorlin syndromeS Levanat, R J Gorlin, S Fallet, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosomeB Levy, P Papenhausen, J Tepperberg, et al.
Pediatric Research|May 1, 1992
Enzyme augmentation in moderate to life-threatening Gaucher diseaseS Fallet, M E Grace, A Sibille, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 6, 2020
Are cuffless devices challenged enough? Design of a validation protocol for ambulatory blood pressure monitors at the wrist: the case of the Aktiia BraceletJ Sola, A Vybornova, S Fallet, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Pediatric Cardiology|April 8, 2000
Patients' age at time of testing for chromosome 22q11 microdeletions: missed opportunities for genetic counselingY Liu, S Fallet, R Koppel
American Journal of Medical Genetics|August 23, 1996
Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literatureR Koppel, S Friedman, S Fallet
American Journal of Medical Genetics|January 23, 1999
Mosaicism with a normal cell line and an unbalanced structural rearrangementA L Zaslav, S Fallet, D Blumenthal, et al.
Prenatal Diagnosis|March 1, 1993
Prenatal detection of monosomy 21 mosaicismA Ghidini, S Fallet, J Robinowitz, et al.
Clinical Genetics|July 3, 1998
Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literatureA L Zaslav, S Fallet, S Brown, et al.
Nature Genetics|January 1, 1996
A two-hit model for developmental defects in Gorlin syndromeS Levanat, R J Gorlin, S Fallet, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosomeB Levy, P Papenhausen, J Tepperberg, et al.
Pediatric Research|May 1, 1992
Enzyme augmentation in moderate to life-threatening Gaucher diseaseS Fallet, M E Grace, A Sibille, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 6, 2020
Are cuffless devices challenged enough? Design of a validation protocol for ambulatory blood pressure monitors at the wrist: the case of the Aktiia BraceletJ Sola, A Vybornova, S Fallet, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Pageof 1