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Alasdair Hunter

Showing results (1-10 of 9) with videos related to

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Pediatric Pulmonology|April 18, 2006
Horseshoe lung and facio-auriculo-vertebral sequence: a previously unreported associationLisa D'Alessandro, Tom Kovesi, Sherief Massoud, et al.
American Journal of Medical Genetics. Part A|January 20, 2009
Elements of morphology: standard terminology for the earAlasdair Hunter, Jaime L Frias, Gabriele Gillessen-Kaesbach, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutationsJoanna McCauley, Navta Masand, Ruth McGowan, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndromeJacques Rochette, Patrice Roll, Ying-Hui Fu, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Neurology|October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraineRobin Cloarec, Nadine Bruneau, Gabrielle Rudolf, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Further delineation of Kabuki syndrome in 48 well-defined new individualsLinlea Armstrong, Azza Abd El Moneim, Kirk Aleck, et al.
American Journal of Medical Genetics. Part A|February 8, 2024
Personal journeys to and in human genetics and dysmorphologyCharles E Schwartz, Arthur S Aylsworth, Judith Allanson, et al.
Human Mutation|January 4, 2012
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific databaseMatthew Bower, Rémi Salomon, Judith Allanson, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Pediatric Pulmonology|April 18, 2006
Horseshoe lung and facio-auriculo-vertebral sequence: a previously unreported associationLisa D'Alessandro, Tom Kovesi, Sherief Massoud, et al.
American Journal of Medical Genetics. Part A|January 20, 2009
Elements of morphology: standard terminology for the earAlasdair Hunter, Jaime L Frias, Gabriele Gillessen-Kaesbach, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutationsJoanna McCauley, Navta Masand, Ruth McGowan, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndromeJacques Rochette, Patrice Roll, Ying-Hui Fu, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Neurology|October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraineRobin Cloarec, Nadine Bruneau, Gabrielle Rudolf, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Further delineation of Kabuki syndrome in 48 well-defined new individualsLinlea Armstrong, Azza Abd El Moneim, Kirk Aleck, et al.
American Journal of Medical Genetics. Part A|February 8, 2024
Personal journeys to and in human genetics and dysmorphologyCharles E Schwartz, Arthur S Aylsworth, Judith Allanson, et al.
Human Mutation|January 4, 2012
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific databaseMatthew Bower, Rémi Salomon, Judith Allanson, et al.
Pageof 1