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Medicina Clinica, ISSN 0025-7753, 2007, Volume 128, Issue 4, pp. 137 - 140
El síndrome de Dyggve-Melchior-Clausen es una displasia espondiloepimetafisaria progresiva, que se caracteriza por enanismo con tronco corto, tórax ancho,... 
Mutations | Smith-McCort syndrome (SMC) | Mutaciones | Haplotipo | Síndrome de Dyggve-Melchior-Clausen (DMC) | Síndrome de Smith-McCort (SMC) | Dyggve-Melchior-Clausen syndrome (DMC) | Haplotype
Journal Article
Human mutation, ISSN 1059-7794, 08/2019
Campomelic dysplasia (CD) is an autosomal dominant, perinatal lethal skeletal dysplasia characterized by a small chest and short long bones with bowing of the... 
Journal Article
BMC Genomics, ISSN 1471-2164, 12/2017, Volume 18, Issue 1, pp. 983 - 15
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 05/2013, Volume 368, Issue 19, pp. 1809 - 1816
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 11/2013, Volume 93, Issue 5, pp. 926 - 931
Short-rib polydactyly (SRP) syndrome type III, or Verma-Naumoff syndrome, is an autosomal-recessive chondrodysplasia characterized by short ribs, a narrow... 
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2019, Volume 179, Issue 8, p. 1672
Journal Article
Journal Article
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 08/2014, Volume 29, Issue 8, pp. 1815 - 1822
Journal Article
Journal Article