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pro vyhledávání: '"Harakiran Nistala"'
Autor:
Harakiran Nistala, David M. Valenzuela, George D. Yancopoulos, Lisa Stadmeyer, Elizabetta Gazzerro, Florian Witte, Renata C. Pereira, Lori C. Gowen, Regina Raz, Stefan Mundlos, Stephanie M. Zabski, Julie L. Clor, Mark W. Sleeman, Ernesto Canalis, Sigmar Stricker, Xiangmin Wang, Aris N. Economides
Publikováno v:
Development (Cambridge, England). 135(9)
Mutations in ROR2 result in a spectrum of genetic disorders in humans that are classified, depending on the nature of the mutation and the clinical phenotype, as either autosomal dominant brachydactyly type B (BDB,MIM 113000) or recessive Robinow syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::642b92ea021d314630a14609e4eec271
https://pubmed.ncbi.nlm.nih.gov/18353862
https://pubmed.ncbi.nlm.nih.gov/18353862
