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Cynthia M Powell

Showing results (11-20 of 65) with videos related to

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American Journal of Medical Genetics. Part A|July 18, 2009
Prenatal diagnosis of mosaic complete trisomy 1qColleen L Schmitt, Julie S Moldenhauer, Honor Wolfe, et al.
Pediatrics in Review|May 1, 2021
Klinefelter Syndrome and Turner SyndromeCarole Samango-Sprouse, Sophia Q Song, Angela E Lin, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Mild achondroplasia/hypochondroplasia with acanthosis nigricans, normal development, and a p.Ser348Cys FGFR3 mutationNatario L Couser, Chetna K Pande, Christie M Turcott, et al.
Maternal and Child Health Journal|May 20, 2020
Parental Views on Newborn Next Generation Sequencing: Implications for Decision SupportRebecca R Moultrie, Ryan Paquin, Christine Rini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Training the next generation of genomic medicine providers: trends in medical education and national assessmentShoumita Dasgupta, Gerald L Feldman, Cynthia M Powell, et al.
Pediatrics|August 18, 2017
Fragile X Newborn Screening: Lessons Learned From a Multisite Screening StudyDonald B Bailey, Elizabeth Berry-Kravis, Louise W Gane, et al.
Archives of Oral Biology|May 17, 2005
Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfectaDarren B Ravassipour, Cynthia M Powell, Ceib L Phillips, et al.
Archives of Otolaryngology--Head & Neck Surgery|October 20, 2010
Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalitiesJane W Kimani, Craig A Buchman, Jessica K Booker, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermiaDemetra S Stamm, Arthur S Aylsworth, Jeffrey M Stajich, et al.
Pediatrics|July 15, 2015
Maternal Consequences of the Detection of Fragile X Carriers in Newborn ScreeningDonald B Bailey, Anne Wheeler, Elizabeth Berry-Kravis, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|July 18, 2009
Prenatal diagnosis of mosaic complete trisomy 1qColleen L Schmitt, Julie S Moldenhauer, Honor Wolfe, et al.
Pediatrics in Review|May 1, 2021
Klinefelter Syndrome and Turner SyndromeCarole Samango-Sprouse, Sophia Q Song, Angela E Lin, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Mild achondroplasia/hypochondroplasia with acanthosis nigricans, normal development, and a p.Ser348Cys FGFR3 mutationNatario L Couser, Chetna K Pande, Christie M Turcott, et al.
Maternal and Child Health Journal|May 20, 2020
Parental Views on Newborn Next Generation Sequencing: Implications for Decision SupportRebecca R Moultrie, Ryan Paquin, Christine Rini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Training the next generation of genomic medicine providers: trends in medical education and national assessmentShoumita Dasgupta, Gerald L Feldman, Cynthia M Powell, et al.
Pediatrics|August 18, 2017
Fragile X Newborn Screening: Lessons Learned From a Multisite Screening StudyDonald B Bailey, Elizabeth Berry-Kravis, Louise W Gane, et al.
Archives of Oral Biology|May 17, 2005
Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfectaDarren B Ravassipour, Cynthia M Powell, Ceib L Phillips, et al.
Archives of Otolaryngology--Head & Neck Surgery|October 20, 2010
Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalitiesJane W Kimani, Craig A Buchman, Jessica K Booker, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermiaDemetra S Stamm, Arthur S Aylsworth, Jeffrey M Stajich, et al.
Pediatrics|July 15, 2015
Maternal Consequences of the Detection of Fragile X Carriers in Newborn ScreeningDonald B Bailey, Anne Wheeler, Elizabeth Berry-Kravis, et al.
Pageof 7