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J H Smith

Showing results (391-400 of 588) with videos related to

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Archives of Disease in Childhood. Fetal and Neonatal Edition|August 24, 2004
Predicting outcome in ex-premature infants supported with extracorporeal membrane oxygenation for acute hypoxic respiratory failureK L Brown, G Walker, D J Grant, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 8, 2004
Metalloprotease-disintegrin ADAM8: expression analysis and targeted deletion in miceKristine Kelly, Gillian Hutchinson, Daniela Nebenius-Oosthuizen, et al.
European Journal of Pediatrics|September 25, 2008
Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairmentKimia Kahrizi, Marzieh Mohseni, Carla Nishimura, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 22, 2016
C4 Glomerulopathy: A Disease Entity Associated With C4d DepositionSanjeev Sethi, Patrick S Quint, Conall M O'Seaghdha, et al.
Prenatal Diagnosis|January 1, 1991
Cytogenetic studies of amniotic fluid taken before the 15th week of pregnancy for earlier prenatal diagnosis: a report of 114 consecutive casesM T Rebello, C T Gray, D E Rooney, et al.
International Journal of Pediatric Otorhinolaryngology|December 4, 2003
GJB2 gene mutations causing familial hereditary deafness in TurkeyYildirim A Bayazit, Benjamin B Cable, Osman Cataloluk, et al.
Human Mutation|September 15, 2004
GJB2: the spectrum of deafness-causing allele variants and their phenotypeHela Azaiez, G Parker Chamberlin, Stephanie M Fischer, et al.
Journal of Human Genetics|April 12, 2007
A novel DFNA5 mutation does not cause hearing loss in an Iranian familyLut Van Laer, Nicole C Meyer, Mahdi Malekpour, et al.
Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing lossHideaki Moteki, A Eliot Shearer, Shuji Izumi, et al.
Pageof 59

Showing results (391-400 of 588) with videos related to

Sort By:
Pageof 59
Archives of Disease in Childhood. Fetal and Neonatal Edition|August 24, 2004
Predicting outcome in ex-premature infants supported with extracorporeal membrane oxygenation for acute hypoxic respiratory failureK L Brown, G Walker, D J Grant, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 8, 2004
Metalloprotease-disintegrin ADAM8: expression analysis and targeted deletion in miceKristine Kelly, Gillian Hutchinson, Daniela Nebenius-Oosthuizen, et al.
European Journal of Pediatrics|September 25, 2008
Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairmentKimia Kahrizi, Marzieh Mohseni, Carla Nishimura, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 22, 2016
C4 Glomerulopathy: A Disease Entity Associated With C4d DepositionSanjeev Sethi, Patrick S Quint, Conall M O'Seaghdha, et al.
Prenatal Diagnosis|January 1, 1991
Cytogenetic studies of amniotic fluid taken before the 15th week of pregnancy for earlier prenatal diagnosis: a report of 114 consecutive casesM T Rebello, C T Gray, D E Rooney, et al.
International Journal of Pediatric Otorhinolaryngology|December 4, 2003
GJB2 gene mutations causing familial hereditary deafness in TurkeyYildirim A Bayazit, Benjamin B Cable, Osman Cataloluk, et al.
Human Mutation|September 15, 2004
GJB2: the spectrum of deafness-causing allele variants and their phenotypeHela Azaiez, G Parker Chamberlin, Stephanie M Fischer, et al.
Journal of Human Genetics|April 12, 2007
A novel DFNA5 mutation does not cause hearing loss in an Iranian familyLut Van Laer, Nicole C Meyer, Mahdi Malekpour, et al.
Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing lossHideaki Moteki, A Eliot Shearer, Shuji Izumi, et al.
Pageof 59