Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Virginia K Proud

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
American Journal of Medical Genetics. Part A|September 17, 2008
Hardikar syndrome: new featuresJ Rainer Poley, Virginia K Proud
American Journal of Medical Genetics. Part A|March 17, 2009
Polyhydramnios, fetal overgrowth, and macrocephaly: prenatal ultrasound findings of Costello syndromeLaura P Smith, John Podraza, Virginia K Proud
Obstetrics and Gynecology|January 23, 2010
Avoiding transmitting identified mutations to offspring using preimplantation genetic diagnosisLaura P Smith, Mark R Hughes, Ilango Thirumoorthi, et al.
Journal of Pediatric Genetics|September 15, 2016
Advancing our understanding of the inheritance and transmission of pectus excavatumLisa Horth, Michael W Stacey, Virginia K Proud, et al.
Pediatric Radiology|April 24, 2003
Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic featuresStephen F Miller, Virginia K Proud, Alice L Werner, et al.
Journal of Pediatric Surgery|September 6, 2006
Classification of the dysmorphology of pectus excavatumMark J Cartoski, Donald Nuss, Michael J Goretsky, et al.
Journal of Pediatric Surgery|October 3, 2006
Family study of the inheritance of pectus excavatumHeather A Creswick, Michael W Stacey, Robert E Kelly, et al.
American Journal of Medical Genetics. Part A|October 17, 2006
Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8Reha M Toydemir, Harold Chen, Virginia K Proud, et al.
American Journal of Medical Genetics. Part A|March 3, 2015
Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III)David D Weaver, Audrey R Norby, Jill A Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|September 17, 2008
Hardikar syndrome: new featuresJ Rainer Poley, Virginia K Proud
American Journal of Medical Genetics. Part A|March 17, 2009
Polyhydramnios, fetal overgrowth, and macrocephaly: prenatal ultrasound findings of Costello syndromeLaura P Smith, John Podraza, Virginia K Proud
Obstetrics and Gynecology|January 23, 2010
Avoiding transmitting identified mutations to offspring using preimplantation genetic diagnosisLaura P Smith, Mark R Hughes, Ilango Thirumoorthi, et al.
Journal of Pediatric Genetics|September 15, 2016
Advancing our understanding of the inheritance and transmission of pectus excavatumLisa Horth, Michael W Stacey, Virginia K Proud, et al.
Pediatric Radiology|April 24, 2003
Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic featuresStephen F Miller, Virginia K Proud, Alice L Werner, et al.
Journal of Pediatric Surgery|September 6, 2006
Classification of the dysmorphology of pectus excavatumMark J Cartoski, Donald Nuss, Michael J Goretsky, et al.
Journal of Pediatric Surgery|October 3, 2006
Family study of the inheritance of pectus excavatumHeather A Creswick, Michael W Stacey, Robert E Kelly, et al.
American Journal of Medical Genetics. Part A|October 17, 2006
Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8Reha M Toydemir, Harold Chen, Virginia K Proud, et al.
American Journal of Medical Genetics. Part A|March 3, 2015
Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III)David D Weaver, Audrey R Norby, Jill A Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Pageof 2