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
An autosomal recessive form of hypophosphatemia (ARHP) was recently shown to be caused by homozygous...
Abstract.- Osteoporosis, a major public health problem, is becoming increasingly prevalent with the ...
Copyright © 2002 Oxford University PressIdiopathic hyperphosphatasia is an autosomal recessive bone ...
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short...
Mutations in LTBP3 are associated with Dental Anomalies and Short Stature syndrome (DASS; MIM 601216...
Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of to...
To present current views that are pertinent to the investigation of the genetic etiology of Class II...
Class III malocclusion is one of the dentofacial deformities that represents a challenge for orthodo...
Abstract Oligodontia is the congenital absence of six or more teeth and comprises the more severe fo...
The process of tooth formation is a series of reciprocal interactions between the ectoderm and mesod...
Abdulaziz Alsemari,1 Mohanned Alsuhaibani,2 Rawabi Alhathlool,1 Bayan Mamdouh Ali1 1Department of Ne...
Osteoporosis is a complex disease that affects >10 million people in the United States and results i...
Osteoporosis pseudoglioma syndrome (OPPG) is an autosomal recessive disorder due to mutations in the...
Osteopoikilosis, Buschke-Ollendorff syndrome (BOS) and melorheostosis are disorders characterized by...
BACKGROUND: Wnt and Wnt-associated pathways play an important role in the genetic etiology of oligod...
An autosomal recessive form of hypophosphatemia (ARHP) was recently shown to be caused by homozygous...
Abstract.- Osteoporosis, a major public health problem, is becoming increasingly prevalent with the ...
Copyright © 2002 Oxford University PressIdiopathic hyperphosphatasia is an autosomal recessive bone ...
We have identified a consanguineous Pakistani family where oligodontia is inherited along with short...
Mutations in LTBP3 are associated with Dental Anomalies and Short Stature syndrome (DASS; MIM 601216...
Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of to...
To present current views that are pertinent to the investigation of the genetic etiology of Class II...
Class III malocclusion is one of the dentofacial deformities that represents a challenge for orthodo...
Abstract Oligodontia is the congenital absence of six or more teeth and comprises the more severe fo...
The process of tooth formation is a series of reciprocal interactions between the ectoderm and mesod...
Abdulaziz Alsemari,1 Mohanned Alsuhaibani,2 Rawabi Alhathlool,1 Bayan Mamdouh Ali1 1Department of Ne...
Osteoporosis is a complex disease that affects >10 million people in the United States and results i...
Osteoporosis pseudoglioma syndrome (OPPG) is an autosomal recessive disorder due to mutations in the...
Osteopoikilosis, Buschke-Ollendorff syndrome (BOS) and melorheostosis are disorders characterized by...
BACKGROUND: Wnt and Wnt-associated pathways play an important role in the genetic etiology of oligod...
An autosomal recessive form of hypophosphatemia (ARHP) was recently shown to be caused by homozygous...
Abstract.- Osteoporosis, a major public health problem, is becoming increasingly prevalent with the ...
Copyright © 2002 Oxford University PressIdiopathic hyperphosphatasia is an autosomal recessive bone ...