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Oncology Letters, ISSN 1792-1074, 01/2016, Volume 11, Issue 1, pp. 105 - 110
Journal Article
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, ISSN 0021-9355, 12/2011, Volume 93A, Issue 24, pp. 2294 - 2302
Background: Multiple hereditary exostoses is an autosomal dominant skeletal disorder characterized by wide variation in clinical phenotype. The aim of this... 
PERFORMANCE LIQUID-CHROMATOGRAPHY | SURGERY | OSTEOCHONDROMAS | CHONDROSARCOMA | MUTATION | DISEASE | HEPARAN-SULFATE | CHROMOSOME-11 | NATURAL-HISTORY | ORTHOPEDICS | HETEROZYGOSITY | EXT2 GENES
Journal Article
Journal of Pediatric Genetics, ISSN 2146-4596, 09/2018, Volume 7, Issue 3, pp. 122 - 124
Abstract Multiple hereditary exostoses (MHE) is a rare disease with autosomal dominant inheritance, caused by heterozygous germline mutations in the EXT1 or... 
Case Report | EXT1 | EXT2 | children | hereditary multiple exostoses | osteochondroma
Journal Article
Prague medical report, ISSN 1214-6994, 01/2017, Volume 118, Issue 2-3, pp. 87 - 94
Hereditary multiple exostoses (HME) represents a heterogeneous group of diseases often associated with progressive skeletal deformities. Most frequently,... 
EXT1 | EXT2 | Multiple exostoses | Index Medicus
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 05/2019, Volume 36, Issue 5, pp. 451 - 455
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2000, Volume 97, Issue 2, pp. 668 - 673
Journal Article
Cell Reports, ISSN 2211-1247, 01/2015, Volume 10, Issue 3, pp. 414 - 428
Collective cell migration is a highly regulated morphogenetic movement during embryonic development and cancer invasion that involves the precise orchestration... 
WNT/BETA-CATENIN | GLYPICAN | DISEASE | SURFACE | MOLECULAR PATHOGENESIS | FIBROBLAST-GROWTH-FACTOR | POSTERIOR LATERAL-LINE | ZEBRAFISH EXT2 | TISSUE MIGRATION | HSPG SYNTHESIS | CELL BIOLOGY
Journal Article
Clinical Genetics, ISSN 0009-9163, 01/2019, Volume 95, Issue 1, pp. 165 - 171
Biallelic exostosin‐2 ( EXT2 ) pathogenic variants have been described as the cause of the Seizures‐Scoliosis‐Macrocephaly syndrome (OMIM 616682) characterized... 
multiple exostoses | AREXT2 syndrome | EXT2 | heparan sulfate | SSM syndrome | EXT1 | GENE | GENETICS & HEREDITY | MUTATIONS | Family | Genetic aspects | Genetic disorders | Seizures (Medicine) | Sulfates | Heparan sulfate | Phenotypes | Proteoglycans | Scoliosis | Heparan sulfate proteoglycans | Glycosylation | Bone diseases | Genotypes | Seizures
Journal Article
Applied Mechanics and Materials, ISSN 1660-9336, 2013, Volume 380-384, pp. 2195 - 2199
  This paper discusses about types of file structures in Linux, points out that EXT2 is the most commonly used file system in Linux, analyzes the disk layout,... 
EXT2 | Inode | File directory | Linux | Compound index
Conference Proceeding
Matrix Biology, ISSN 0945-053X, 04/2014, Volume 35, pp. 25 - 33
Journal Article
Developmental Cell, ISSN 1534-5807, 08/2011, Volume 21, Issue 2, pp. 257 - 272
Journal Article