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Antony E Shrimpton

Showing results (1-10 of 19) with videos related to

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Expert Review of Molecular Diagnostics|June 8, 2002
Molecular diagnosis of cystic fibrosisAntony E Shrimpton
European Journal of Medical Genetics|February 25, 2006
A TNNI2 mutation in a family with distal arthrogryposis type 2BAntony E Shrimpton, Joe J Hoo
American Journal of Medical Genetics. Part A|November 20, 2004
Familial hyper- and hypopigmentation with age-related pattern changeJoe J Hoo, Antony E Shrimpton
American Journal of Medical Genetics. Part A|January 19, 2008
Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delayJoe J Hoo, Antony E Shrimpton
Genetic Testing|June 25, 2003
Cystic fibrosis: S158N (605G --> A) is a rare genetic variant found in coupling with deltaF508Karen Hicks, Wendy Beadling, Antony E Shrimpton
American Journal of Medical Genetics. Part A|January 18, 2006
Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficitAntony E Shrimpton, Kimberly A Jensen, Joe J Hoo
BMC Bioinformatics|July 25, 2015
GESPA: classifying nsSNPs to predict disease associationJay K Khurana, Jay E Reeder, Antony E Shrimpton, et al.
Skeletal Radiology|September 16, 2004
Congenital vertical talus in four generations of the same familyE Mark Levinsohn, Antony E Shrimpton, Robert B Cady, et al.
American Journal of Clinical Pathology|August 25, 2004
A new HLA-A1 mutation: a novel, null variant alleleJohn Bernard Henry, Charlene A Hubbell, Mary C Davis, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 25, 2007
A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesisAntony E Shrimpton, Robert L Schelper, Reinhold P Linke, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Expert Review of Molecular Diagnostics|June 8, 2002
Molecular diagnosis of cystic fibrosisAntony E Shrimpton
European Journal of Medical Genetics|February 25, 2006
A TNNI2 mutation in a family with distal arthrogryposis type 2BAntony E Shrimpton, Joe J Hoo
American Journal of Medical Genetics. Part A|November 20, 2004
Familial hyper- and hypopigmentation with age-related pattern changeJoe J Hoo, Antony E Shrimpton
American Journal of Medical Genetics. Part A|January 19, 2008
Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delayJoe J Hoo, Antony E Shrimpton
Genetic Testing|June 25, 2003
Cystic fibrosis: S158N (605G --> A) is a rare genetic variant found in coupling with deltaF508Karen Hicks, Wendy Beadling, Antony E Shrimpton
American Journal of Medical Genetics. Part A|January 18, 2006
Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficitAntony E Shrimpton, Kimberly A Jensen, Joe J Hoo
BMC Bioinformatics|July 25, 2015
GESPA: classifying nsSNPs to predict disease associationJay K Khurana, Jay E Reeder, Antony E Shrimpton, et al.
Skeletal Radiology|September 16, 2004
Congenital vertical talus in four generations of the same familyE Mark Levinsohn, Antony E Shrimpton, Robert B Cady, et al.
American Journal of Clinical Pathology|August 25, 2004
A new HLA-A1 mutation: a novel, null variant alleleJohn Bernard Henry, Charlene A Hubbell, Mary C Davis, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 25, 2007
A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesisAntony E Shrimpton, Robert L Schelper, Reinhold P Linke, et al.
Pageof 2