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Angela E Lin

Showing results (81-90 of 170) with videos related to

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Birth Defects Research. Part A, Clinical and Molecular Teratology|April 4, 2007
Maternal caffeine consumption and risk of cardiovascular malformationsMarilyn L Browne, Erin M Bell, Charlotte M Druschel, et al.
American Journal of Medical Genetics. Part A|August 8, 2014
Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiologyAngela E Lin, Sergey Krikov, Tiffany Riehle-Colarusso, et al.
American Journal of Medical Genetics. Part A|September 1, 2023
Atlantoaxial instability associated with ALDH18A1 mutationAlexandra T Lucas, Angela E Lin, Andrew Cohen, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patientsAngela E Lin, Avram Z Traum, Inderneel Sahai, et al.
American Journal of Medical Genetics|February 22, 2002
Five additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocolKaren W Gripp, Charles I Scott, Linda Nicholson, et al.
European Journal of Medical Genetics|March 29, 2014
Turner syndrome and meningioma: support for a possible increased risk of neoplasia in Turner syndromeDanielle B Pier, Fabio P Nunes, Scott R Plotkin, et al.
Pediatrics|May 28, 2008
Turner syndrome is an independent risk factor for aortic dilation in the youngLeo Lopez, Kristopher L Arheart, Steven D Colan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND geneTaosheng Huang, Angela E Lin, Gerald F Cox, et al.
Birth Defects Research|March 12, 2022
Patterns of multiple congenital anomalies in the National Birth Defect Prevention Study: Challenges and insightsMeredith M Howley, Eva Williford, A J Agopian, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|September 19, 2022
Review of the Pathologic Characteristics in Myhre Syndrome: Gain-of-Function Pathogenic Variants in <i>SMAD4</i> cause a Multisystem Fibroproliferative ResponseLois J Starr, Mark E Lindsay, Deborah Perry, et al.
Pageof 17

Showing results (81-90 of 170) with videos related to

Sort By:
Pageof 17
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 4, 2007
Maternal caffeine consumption and risk of cardiovascular malformationsMarilyn L Browne, Erin M Bell, Charlotte M Druschel, et al.
American Journal of Medical Genetics. Part A|August 8, 2014
Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiologyAngela E Lin, Sergey Krikov, Tiffany Riehle-Colarusso, et al.
American Journal of Medical Genetics. Part A|September 1, 2023
Atlantoaxial instability associated with ALDH18A1 mutationAlexandra T Lucas, Angela E Lin, Andrew Cohen, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patientsAngela E Lin, Avram Z Traum, Inderneel Sahai, et al.
American Journal of Medical Genetics|February 22, 2002
Five additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocolKaren W Gripp, Charles I Scott, Linda Nicholson, et al.
European Journal of Medical Genetics|March 29, 2014
Turner syndrome and meningioma: support for a possible increased risk of neoplasia in Turner syndromeDanielle B Pier, Fabio P Nunes, Scott R Plotkin, et al.
Pediatrics|May 28, 2008
Turner syndrome is an independent risk factor for aortic dilation in the youngLeo Lopez, Kristopher L Arheart, Steven D Colan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND geneTaosheng Huang, Angela E Lin, Gerald F Cox, et al.
Birth Defects Research|March 12, 2022
Patterns of multiple congenital anomalies in the National Birth Defect Prevention Study: Challenges and insightsMeredith M Howley, Eva Williford, A J Agopian, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|September 19, 2022
Review of the Pathologic Characteristics in Myhre Syndrome: Gain-of-Function Pathogenic Variants in <i>SMAD4</i> cause a Multisystem Fibroproliferative ResponseLois J Starr, Mark E Lindsay, Deborah Perry, et al.
Pageof 17