We have identified a consanguineous Pakistani family where oligodontia is inherited along with short stature in an autosomal-recessive fashion. Increased bone density was present in the spine and at the base of the skull. Using high-density single-nucleotide polymorphism microarrays for homozygosity mapping, we identified a 28 Mb homozygous stretch shared between affected individuals on chromosome 11q13. Screening selected candidate genes within this region, we identified a homozygous nonsense mutation, Y774X, within LTBP3, the gene for the latent TGF-β binding protein 3, an extracellular matrix protein believed to be required for osteoclast function
Osteoporosis is a complex disease that affects >10 million people in the United States and results i...
Tooth agenesis is common dentofacial malformation in humans. Its etiology is still not clear. Hypodo...
The tooth development (odontogenesis) is a complicated and dynamic process involving many proteins. ...
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short...
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short...
Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of to...
Abstract Oligodontia is the congenital absence of six or more teeth and comprises the more severe fo...
Inherited dental malformations constitute a clinically and genetically heterogeneous group of disord...
Class III malocclusion is one of the dentofacial deformities that represents a challenge for orthodo...
Skeletal dysplasias are often well characterized, and only a minority of the cases remain unsolved a...
Tooth agenesis is one of the most common congenital malformations in humans. Hypodontia can either o...
Mutations in LTBP3 are associated with Dental Anomalies and Short Stature syndrome (DASS; MIM 601216...
PhDAn evolution in methods of identifying the causal mutations and candidate genes for Mendelian dis...
Objective: To understand the role of MSX1 gene in Pakistani families with hypodontia. Study Desig...
BACKGROUND: Wnt and Wnt-associated pathways play an important role in the genetic etiology of oligod...
Osteoporosis is a complex disease that affects >10 million people in the United States and results i...
Tooth agenesis is common dentofacial malformation in humans. Its etiology is still not clear. Hypodo...
The tooth development (odontogenesis) is a complicated and dynamic process involving many proteins. ...
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short...
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short...
Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of to...
Abstract Oligodontia is the congenital absence of six or more teeth and comprises the more severe fo...
Inherited dental malformations constitute a clinically and genetically heterogeneous group of disord...
Class III malocclusion is one of the dentofacial deformities that represents a challenge for orthodo...
Skeletal dysplasias are often well characterized, and only a minority of the cases remain unsolved a...
Tooth agenesis is one of the most common congenital malformations in humans. Hypodontia can either o...
Mutations in LTBP3 are associated with Dental Anomalies and Short Stature syndrome (DASS; MIM 601216...
PhDAn evolution in methods of identifying the causal mutations and candidate genes for Mendelian dis...
Objective: To understand the role of MSX1 gene in Pakistani families with hypodontia. Study Desig...
BACKGROUND: Wnt and Wnt-associated pathways play an important role in the genetic etiology of oligod...
Osteoporosis is a complex disease that affects >10 million people in the United States and results i...
Tooth agenesis is common dentofacial malformation in humans. Its etiology is still not clear. Hypodo...
The tooth development (odontogenesis) is a complicated and dynamic process involving many proteins. ...