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F Sessions Cole

Showing results (21-30 of 101) with videos related to

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Pediatric Research|March 15, 2018
Mutations in the thyroid transcription factor gene NKX2-1 result in decreased expression of SFTPB and SFTPCStephanie J Attarian, Sandra L Leibel, Ping Yang, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndromeKimberly I Mills, Jacqueline Anderson, Philip T Levy, et al.
American Journal of Perinatology|November 29, 2017
Neonatal Outcomes Differ after Spontaneous and Indicated Preterm BirthMolly J Stout, Devyn Demaree, Emily Merfeld, et al.
Bone|March 28, 2019
Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiencyCarla Sandler-Wilson, Jennifer A Wambach, Bess A Marshall, et al.
Pediatric Research|February 17, 2012
An intronic ABCA3 mutation that is responsible for respiratory diseaseAmit Agrawal, Aaron Hamvas, F Sessions Cole, et al.
BMC Medical Genetics|October 10, 2013
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotypeEline van Meel, Daniel J Wegner, Paul Cliften, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 27, 2018
Addressing medically underserved populations through maternal-fetal transport: a geographic analysisJoshua I Rosenbloom, D Michael Nelson, Scott Saunders, et al.
The Journal of Pediatrics|July 27, 2020
The Challenge of Risk Stratification of Infants Born Preterm in the Setting of Competing and Disparate Healthcare OutcomesHalana V Whitehead, Christopher C McPherson, Zachary A Vesoulis, et al.
Archives of Pediatrics & Adolescent Medicine|June 9, 2004
Informed consent for genetic researchAaron Hamvas, Katherine K Madden, Lawrence M Nogee, et al.
American Journal of Respiratory and Critical Care Medicine|February 19, 2025
Interstitial Lung Disease and Lung Cancer Associated with a Monoallelic Novel Variant in <i>SFTPB</i>Jennifer A Wambach, Lawrence M Nogee, David R Spielberg, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
Pediatric Research|March 15, 2018
Mutations in the thyroid transcription factor gene NKX2-1 result in decreased expression of SFTPB and SFTPCStephanie J Attarian, Sandra L Leibel, Ping Yang, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndromeKimberly I Mills, Jacqueline Anderson, Philip T Levy, et al.
American Journal of Perinatology|November 29, 2017
Neonatal Outcomes Differ after Spontaneous and Indicated Preterm BirthMolly J Stout, Devyn Demaree, Emily Merfeld, et al.
Bone|March 28, 2019
Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiencyCarla Sandler-Wilson, Jennifer A Wambach, Bess A Marshall, et al.
Pediatric Research|February 17, 2012
An intronic ABCA3 mutation that is responsible for respiratory diseaseAmit Agrawal, Aaron Hamvas, F Sessions Cole, et al.
BMC Medical Genetics|October 10, 2013
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotypeEline van Meel, Daniel J Wegner, Paul Cliften, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 27, 2018
Addressing medically underserved populations through maternal-fetal transport: a geographic analysisJoshua I Rosenbloom, D Michael Nelson, Scott Saunders, et al.
The Journal of Pediatrics|July 27, 2020
The Challenge of Risk Stratification of Infants Born Preterm in the Setting of Competing and Disparate Healthcare OutcomesHalana V Whitehead, Christopher C McPherson, Zachary A Vesoulis, et al.
Archives of Pediatrics & Adolescent Medicine|June 9, 2004
Informed consent for genetic researchAaron Hamvas, Katherine K Madden, Lawrence M Nogee, et al.
American Journal of Respiratory and Critical Care Medicine|February 19, 2025
Interstitial Lung Disease and Lung Cancer Associated with a Monoallelic Novel Variant in <i>SFTPB</i>Jennifer A Wambach, Lawrence M Nogee, David R Spielberg, et al.
Pageof 11