Funder
Gobierno de España Ministerio de Ciencia e Innovación
Subject
Genetics(clinical),Genetics,General Medicine
Reference17 articles.
1. The skeletal phenotype of achondrogeneis type 1A is caused exclusively by cartilage defects;Bird;Development,2018
2. Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity;Bonaventure;Am. J. Med. Genet.,1992
3. Argentine references for the assessment of body proportions from birth to 17 years of age. Referencias argentinas para la evaluación de proporciones corporales desde el nacimiento hasta los 17 años;Del Pino;Arch. Argent. Pediatr.,2017
4. Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfecta;Goldblatt;Am. J. Med. Genet.,1991
5. GMAP-210, A cis-Golgi network-associated protein, is a minus end microtubule binding protein;Infante;J. Cell Biol.,1999
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