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

Elizabeth M Berry-Kravis

Showing results (31-40 of 86) with videos related to

Pageof 9
Sort By:
American Journal of Medical Genetics. Part A|February 25, 2003
Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter geneDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Brion S Maher, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS)Casey M Rand, Min Yu, Lawrence J Jennings, et al.
Disability and Health Journal|May 24, 2019
Preventive care services and health behaviors in children with fragile X syndromeKendra E Gilbertson, Hannah L Jackson, Eric J Dziuban, et al.
Pediatric Pulmonology|August 11, 2011
Variable human phenotype associated with novel deletions of the PHOX2B geneLawrence J Jennings, Min Yu, Casey M Rand, et al.
Psychoneuroendocrinology|May 21, 2021
Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndromeJinkuk Hong, Amita Kapoor, Leann Smith DaWalt, et al.
Pediatric Pulmonology|May 8, 2009
Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicineDebra E Weese-Mayer, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A|January 24, 2019
Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family membersYakov Sivan, Amy Zhou, Lawrence J Jennings, et al.
American Journal of Medical Genetics. Part A|November 11, 2003
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2bDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou, et al.
Pediatric Research|July 9, 2004
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic developmentDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 19, 2008
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B geneGabriela M Repetto, Raul J Corrales, Selim G Abara, et al.
Pageof 9

Showing results (31-40 of 86) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|February 25, 2003
Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter geneDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Brion S Maher, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS)Casey M Rand, Min Yu, Lawrence J Jennings, et al.
Disability and Health Journal|May 24, 2019
Preventive care services and health behaviors in children with fragile X syndromeKendra E Gilbertson, Hannah L Jackson, Eric J Dziuban, et al.
Pediatric Pulmonology|August 11, 2011
Variable human phenotype associated with novel deletions of the PHOX2B geneLawrence J Jennings, Min Yu, Casey M Rand, et al.
Psychoneuroendocrinology|May 21, 2021
Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndromeJinkuk Hong, Amita Kapoor, Leann Smith DaWalt, et al.
Pediatric Pulmonology|May 8, 2009
Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicineDebra E Weese-Mayer, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A|January 24, 2019
Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family membersYakov Sivan, Amy Zhou, Lawrence J Jennings, et al.
American Journal of Medical Genetics. Part A|November 11, 2003
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2bDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou, et al.
Pediatric Research|July 9, 2004
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic developmentDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 19, 2008
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B geneGabriela M Repetto, Raul J Corrales, Selim G Abara, et al.
Pageof 9