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by Woo, EJ and Lee, WJ and Hu, KS and Hwang, JJ
PLOS ONE, ISSN 1932-6203, 10/2015, Volume 10, Issue 10, p. e0140901
Skeletal dysplasias related to genetic etiologies have rarely been reported for past populations. This report presents the skeletal characteristics of an... 
MULTIPLE EPIPHYSEAL DYSPLASIA | ACHONDROPLASIA | HUMERUS VARUS | CHONDRODYSTROPHIC DWARFISM | TUBERCULOSIS | MULTIDISCIPLINARY SCIENCES | THALASSEMIA | GENETIC-HETEROGENEITY | LYSOSOMAL STORAGE DISORDERS | FEATURES | MANIFESTATIONS | Thalassemia - diagnosis | Limb Deformities, Congenital - genetics | Paleontology - methods | Humans | Middle Aged | Tomography, X-Ray Computed | Bone Diseases, Developmental - genetics | Dwarfism - diagnosis | Lordosis - diagnosis | Lysosomal Storage Diseases - diagnosis | Lordosis - genetics | Paleopathology - methods | Osteochondrodysplasias - genetics | Adult | Female | Thalassemia - genetics | Bone Diseases, Developmental - diagnosis | Republic of Korea | Achondroplasia - genetics | Achondroplasia - diagnosis | Lysosomal Storage Diseases - genetics | Musculoskeletal Abnormalities | Osteochondrodysplasias - diagnosis | Dwarfism - genetics | Limb Deformities, Congenital - diagnosis | Radiometric Dating | Archaeology - methods | Bone and Bones - abnormalities | Dwarfism | Complications and side effects | Dysplasia | Care and treatment | Usage | Research | Risk factors | Paleopathology | Congenital diseases | Deformation | Laboratories | Anemia | Developmental biology | Thalassemia | Cultural heritage | Dentistry | Chondrodystrophy | Achondroplasia | Hypochondroplasia | Hemolytic anemia | Tuberculosis | Computed tomography | Cemeteries | Etiology | Bone dysplasia | Bones | Skeleton | Diagnosis
Journal Article
European journal of human genetics, ISSN 1018-4813, 2012, Volume 20, Issue 6, pp. 598 - 606
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2017, Volume 16, Issue 6, pp. 417 - 418
[...]she possibly had Kniest dysplasia or another metatropic dwarfism. 
Neurology | NEUROFIBROMATOSIS | CLINICAL NEUROLOGY | HISTORY | Paintings - history | Neurofibromatosis 1 | History, 15th Century | Face | Humans | Dwarfism | Dysplasia
Journal Article
Journal of Maternal-Fetal and Neonatal Medicine, ISSN 1476-7058, 12/2017, Volume 32, Issue 11, pp. 1 - 4
Background: The Seckel syndrome is an autosomal recessive inherited disorder that characterized severe pre- and post-natal growth restriction, microcephaly and... 
microcephaly | Seckel syndrome | A bird-headed appearance | prenatal diagnosis | PRIMORDIAL DWARFISM | OBSTETRICS & GYNECOLOGY
Journal Article
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 01/2018, Volume 102, Issue 1, pp. 27 - 43
Journal Article