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Nancy Vegas

Showing results (11-20 of 18) with videos related to

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Brain : a Journal of Neurology|December 22, 2020
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeNancy Vegas, Karen Low, Christopher C Y Mak, et al.
European Journal of Medical Genetics|October 1, 2018
Mutations in TBR1 gene leads to cortical malformations and intellectual disabilityNancy Vegas, Mara Cavallin, Tjitske Kleefstra, et al.
European Journal of Pediatrics|May 8, 2026
Pulse oximetry in infants with Robin sequenceSonia Khirani, Adrien Kerfourn, Lucie Griffon, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 22, 2026
Development and validation of the new French ORALQUEST scale for evaluating feeding difficulties in young childrenBéatrice Thouvenin, Redha Ould-Ammar, Lisa Ouss, et al.
Orphanet Journal of Rare Diseases|October 21, 2021
Quality of life and phonatory and morphological outcomes in cognitively unimpaired adolescents with Pierre Robin sequence: a cross-sectional study of 72 patientsBéatrice Thouvenin, Véronique Soupre, Marie-Anne Caillaud, et al.
Neurology. Genetics|December 12, 2018
Delineating <i>FOXG1</i> syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.
Human Mutation|February 16, 2022
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published casesNancy Vegas, Zeynep Demir, Christopher T Gordon, et al.
Brain : a Journal of Neurology|December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsisChristopher C Y Mak, Dan Doherty, Angela E Lin, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Brain : a Journal of Neurology|December 22, 2020
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeNancy Vegas, Karen Low, Christopher C Y Mak, et al.
European Journal of Medical Genetics|October 1, 2018
Mutations in TBR1 gene leads to cortical malformations and intellectual disabilityNancy Vegas, Mara Cavallin, Tjitske Kleefstra, et al.
European Journal of Pediatrics|May 8, 2026
Pulse oximetry in infants with Robin sequenceSonia Khirani, Adrien Kerfourn, Lucie Griffon, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 22, 2026
Development and validation of the new French ORALQUEST scale for evaluating feeding difficulties in young childrenBéatrice Thouvenin, Redha Ould-Ammar, Lisa Ouss, et al.
Orphanet Journal of Rare Diseases|October 21, 2021
Quality of life and phonatory and morphological outcomes in cognitively unimpaired adolescents with Pierre Robin sequence: a cross-sectional study of 72 patientsBéatrice Thouvenin, Véronique Soupre, Marie-Anne Caillaud, et al.
Neurology. Genetics|December 12, 2018
Delineating <i>FOXG1</i> syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.
Human Mutation|February 16, 2022
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published casesNancy Vegas, Zeynep Demir, Christopher T Gordon, et al.
Brain : a Journal of Neurology|December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsisChristopher C Y Mak, Dan Doherty, Angela E Lin, et al.
Pageof 2