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Pediatric Pulmonology
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April 18, 2006
Horseshoe lung and facio-auriculo-vertebral sequence: a previously unreported association
Lisa 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 ear
Alasdair 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 mutations
Joanna 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) syndrome
Jacques 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 rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Neurology
|
October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
Robin 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 individuals
Linlea 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 dysmorphology
Charles 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 database
Matthew Bower, Rémi Salomon, Judith Allanson, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Pediatric Pulmonology
|
April 18, 2006
Horseshoe lung and facio-auriculo-vertebral sequence: a previously unreported association
Lisa 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 ear
Alasdair 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 mutations
Joanna 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) syndrome
Jacques 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 rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Neurology
|
October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
Robin 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 individuals
Linlea 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 dysmorphology
Charles 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 database
Matthew Bower, Rémi Salomon, Judith Allanson, et al.
Page
of 1