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Natalie M Gallant

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BMJ Case Reports|February 2, 2018
Neurofibromatosis type 1: a case highlighting pulmonary and other rare clinical manifestationsKhoa Anh Nguyen, Mohamed Elnaggar, Natalie M Gallant, et al.
American Journal of Medical Genetics. Part A|October 14, 2011
Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletionNatalie M Gallant, Erin Baldwin, Noriko Salamon, et al.
Molecular Genetics and Metabolism|October 10, 2013
Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state databaseChristina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
American Journal of Medical Genetics. Part A|January 25, 2019
ALG11-CDG syndrome: Expanding the phenotypeMaria K Haanpää, Bobby G Ng, Natalie M Gallant, et al.
Gene|December 2, 2014
Novel liver findings in ornithine transcarbamylase deficiency due to Xp11.4-p21.1 microdeletionNatalie M Gallant, Dorina Gui, Charles R Lassman, et al.
Journal of Pediatric Hematology/Oncology|February 22, 2019
Hyperammonemia From Ureaplasma Infection in an Immunocompromised ChildNicholas Placone, Roy L Kao, Pamela Kempert, et al.
American Journal of Medical Genetics. Part A|March 16, 2017
De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomaliesSureni V Mullegama, Steven D Klein, Milene V Mulatinho, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Nature Genetics|November 28, 2006
Wnt-beta-catenin signaling initiates taste papilla developmentFei Liu, Shoba Thirumangalathu, Natalie M Gallant, et al.
Developmental Cell|July 22, 2009
Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle inductionYuhang Zhang, Philip Tomann, Thomas Andl, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
BMJ Case Reports|February 2, 2018
Neurofibromatosis type 1: a case highlighting pulmonary and other rare clinical manifestationsKhoa Anh Nguyen, Mohamed Elnaggar, Natalie M Gallant, et al.
American Journal of Medical Genetics. Part A|October 14, 2011
Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletionNatalie M Gallant, Erin Baldwin, Noriko Salamon, et al.
Molecular Genetics and Metabolism|October 10, 2013
Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state databaseChristina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
American Journal of Medical Genetics. Part A|January 25, 2019
ALG11-CDG syndrome: Expanding the phenotypeMaria K Haanpää, Bobby G Ng, Natalie M Gallant, et al.
Gene|December 2, 2014
Novel liver findings in ornithine transcarbamylase deficiency due to Xp11.4-p21.1 microdeletionNatalie M Gallant, Dorina Gui, Charles R Lassman, et al.
Journal of Pediatric Hematology/Oncology|February 22, 2019
Hyperammonemia From Ureaplasma Infection in an Immunocompromised ChildNicholas Placone, Roy L Kao, Pamela Kempert, et al.
American Journal of Medical Genetics. Part A|March 16, 2017
De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomaliesSureni V Mullegama, Steven D Klein, Milene V Mulatinho, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Nature Genetics|November 28, 2006
Wnt-beta-catenin signaling initiates taste papilla developmentFei Liu, Shoba Thirumangalathu, Natalie M Gallant, et al.
Developmental Cell|July 22, 2009
Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle inductionYuhang Zhang, Philip Tomann, Thomas Andl, et al.
Pageof 2