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R E Stevenson

Showing results (71-80 of 126) with videos related to

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American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.
Clinical Genetics|February 1, 1995
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1J C Marinoni, R E Stevenson, J P Evans, et al.
Clinical Genetics|May 8, 2009
Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisisR E Stevenson, R C Rogers, J C Chandler, et al.
American Journal of Medical Genetics|July 9, 1999
XLMR databaseD A Cabezas, J F Arena, R E Stevenson, et al.
Environmental Pollution (Barking, Essex : 1987)|May 26, 2007
Ozone uptake (flux) as it relates to ozone-induced foliar symptoms of Prunus serotina and Populus maximowiziixtrichocarpaT Orendovici-Best, J M Skelly, D D Davis, et al.
Journal of Medical Genetics|June 1, 1997
Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardationR E Stevenson, B Häne, J F Arena, et al.
Clinical Genetics|July 1, 1980
Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6R J Schroer, D M Culp, R E Stevenson, et al.
Pediatrics|October 4, 2000
Decline in prevalence of neural tube defects in a high-risk region of the United StatesR E Stevenson, W P Allen, G S Pai, et al.
American Journal of Human Genetics|September 1, 1990
Allan-Herndon syndrome. I. Clinical studiesR E Stevenson, H O Goodman, C E Schwartz, et al.
Journal of Medical Genetics|June 19, 2002
A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58F E Abidi, E Holinski-Feder, O Rittinger, et al.
Pageof 13

Showing results (71-80 of 126) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.
Clinical Genetics|February 1, 1995
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1J C Marinoni, R E Stevenson, J P Evans, et al.
Clinical Genetics|May 8, 2009
Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisisR E Stevenson, R C Rogers, J C Chandler, et al.
American Journal of Medical Genetics|July 9, 1999
XLMR databaseD A Cabezas, J F Arena, R E Stevenson, et al.
Environmental Pollution (Barking, Essex : 1987)|May 26, 2007
Ozone uptake (flux) as it relates to ozone-induced foliar symptoms of Prunus serotina and Populus maximowiziixtrichocarpaT Orendovici-Best, J M Skelly, D D Davis, et al.
Journal of Medical Genetics|June 1, 1997
Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardationR E Stevenson, B Häne, J F Arena, et al.
Clinical Genetics|July 1, 1980
Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6R J Schroer, D M Culp, R E Stevenson, et al.
Pediatrics|October 4, 2000
Decline in prevalence of neural tube defects in a high-risk region of the United StatesR E Stevenson, W P Allen, G S Pai, et al.
American Journal of Human Genetics|September 1, 1990
Allan-Herndon syndrome. I. Clinical studiesR E Stevenson, H O Goodman, C E Schwartz, et al.
Journal of Medical Genetics|June 19, 2002
A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58F E Abidi, E Holinski-Feder, O Rittinger, et al.
Pageof 13