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Ariane Berdal

Showing results (111-120 of 115) with videos related to

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American Journal of Medical Genetics. Part A|August 31, 2019
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disordersMuriel de La Dure-Molla, Benjamin Philippe Fournier, Maria Cristina Manzanares, et al.
Clinical Genetics|June 2, 2025
A Novel Skeletal Dysplasia With Premaxilla Overgrowth, Gingival Hyperplasia, and Dental HypercementosisPaulo Marcio Yamaguti, Shélida Vasconcelos Braz, Audrey Asselin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 2, 2015
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel FormationClaire Bardet, Frédéric Courson, Yong Wu, et al.
Journal of Medical Genetics|October 28, 2015
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementMegana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Pageof 12

Showing results (111-120 of 115) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 115 results.
American Journal of Medical Genetics. Part A|August 31, 2019
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disordersMuriel de La Dure-Molla, Benjamin Philippe Fournier, Maria Cristina Manzanares, et al.
Clinical Genetics|June 2, 2025
A Novel Skeletal Dysplasia With Premaxilla Overgrowth, Gingival Hyperplasia, and Dental HypercementosisPaulo Marcio Yamaguti, Shélida Vasconcelos Braz, Audrey Asselin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 2, 2015
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel FormationClaire Bardet, Frédéric Courson, Yong Wu, et al.
Journal of Medical Genetics|October 28, 2015
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementMegana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Pageof 12