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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 disorders
Muriel 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 Hypercementosis
Paulo 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 Formation
Claire 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 involvement
Megana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.
Nephron. Physiology
|
February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations
Graciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
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of 12
Search research articles
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Showing results (111-120 of 115) with videos related to
Sort By:
Page
of 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 disorders
Muriel 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 Hypercementosis
Paulo 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 Formation
Claire 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 involvement
Megana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.
Nephron. Physiology
|
February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations
Graciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Page
of 12