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Carol E Anderson

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Journal of Pediatric Endocrinology & Metabolism : JPEM|December 21, 2013
Absence of WNT4 gene mutation in a patient with MURCS associationZohreh Shoar, Tapan Ganguly, Carol E Anderson, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18Carol E Anderson, Hope H Punnett, Vicki Huff, et al.
Journal of Child Neurology|February 25, 2010
5q14.3 deletion manifesting as mitochondrial disease and autism: case reportHerbert Ezugha, Michael Goldenthal, Ignacio Valencia, et al.
American Journal of Medical Genetics. Part A|October 24, 2014
Transposition of the great arteries in a neonate with Klinefelter syndrome-an incidental finding or a true associationJinglan Liu, Achintya Moulick, Cesar I Mesia, et al.
Pediatric Neurology|November 25, 2010
Microarray analysis in children with developmental disorder or epilepsyHerbert Ezugha, Carol E Anderson, Harold G Marks, et al.
Seminars in Pediatric Neurology|August 24, 2014
Fraternal twins with autism, severe cognitive deficit, and epilepsy: diagnostic role of chromosomal microarray analysisJaime Imitola, Diana Walleigh, Carol E Anderson, et al.
Seminars in Pediatric Neurology|August 24, 2014
Brainstem tegmental necrosis and olivary hypoplasia: raising awareness of a rare neuropathologic correlate of congenital apneaChristos D Katsetos, Carol E Anderson, Miguel A Guzman, et al.
Pediatric Blood & Cancer|January 16, 2009
Improvement of pancytopenia and thrombocytopenia with decreasing mosaicism for isochromosome XpS Lauren Gray, J P de Chadarévian, Carol E Anderson, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosisKaren W Gripp, Dina J Zand, Laurie Demmer, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
A report of three patients with an interstitial deletion of chromosome 15q24Lisa J Cushman, Wilfredo Torres-Martinez, Athena M Cherry, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 21, 2013
Absence of WNT4 gene mutation in a patient with MURCS associationZohreh Shoar, Tapan Ganguly, Carol E Anderson, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18Carol E Anderson, Hope H Punnett, Vicki Huff, et al.
Journal of Child Neurology|February 25, 2010
5q14.3 deletion manifesting as mitochondrial disease and autism: case reportHerbert Ezugha, Michael Goldenthal, Ignacio Valencia, et al.
American Journal of Medical Genetics. Part A|October 24, 2014
Transposition of the great arteries in a neonate with Klinefelter syndrome-an incidental finding or a true associationJinglan Liu, Achintya Moulick, Cesar I Mesia, et al.
Pediatric Neurology|November 25, 2010
Microarray analysis in children with developmental disorder or epilepsyHerbert Ezugha, Carol E Anderson, Harold G Marks, et al.
Seminars in Pediatric Neurology|August 24, 2014
Fraternal twins with autism, severe cognitive deficit, and epilepsy: diagnostic role of chromosomal microarray analysisJaime Imitola, Diana Walleigh, Carol E Anderson, et al.
Seminars in Pediatric Neurology|August 24, 2014
Brainstem tegmental necrosis and olivary hypoplasia: raising awareness of a rare neuropathologic correlate of congenital apneaChristos D Katsetos, Carol E Anderson, Miguel A Guzman, et al.
Pediatric Blood & Cancer|January 16, 2009
Improvement of pancytopenia and thrombocytopenia with decreasing mosaicism for isochromosome XpS Lauren Gray, J P de Chadarévian, Carol E Anderson, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosisKaren W Gripp, Dina J Zand, Laurie Demmer, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
A report of three patients with an interstitial deletion of chromosome 15q24Lisa J Cushman, Wilfredo Torres-Martinez, Athena M Cherry, et al.
Pageof 2