Matches in Nanopublications for { ?s ?p "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP552322.RAg028uJ7izqO_h5i0w903u6q9gX-l-i77d1V2rC5MP74130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552322.RAg028uJ7izqO_h5i0w903u6q9gX-l-i77d1V2rC5MP74130_provenance.
- NP214965.RAGi-pSTeGytaKqANbnOtNRsDU2P9Q_pOq3nuqf05sbkQ130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214965.RAGi-pSTeGytaKqANbnOtNRsDU2P9Q_pOq3nuqf05sbkQ130_provenance.
- NP658086.RA39h8sAHJsPp0hPQBDn9Dm4qH6dbyWDIMoWaHMq4OEhA130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658086.RA39h8sAHJsPp0hPQBDn9Dm4qH6dbyWDIMoWaHMq4OEhA130_provenance.
- NP693886.RAUvOnfgwqxsrtgqO0QHCWdHFJ-P7elEetEa4i1OGGDNE130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693886.RAUvOnfgwqxsrtgqO0QHCWdHFJ-P7elEetEa4i1OGGDNE130_provenance.
- assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP760806.RAdhnUR5VawIW0F9qFLfdkAXzRKYQlSY4eOhZR3eNJM84130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760806.RAdhnUR5VawIW0F9qFLfdkAXzRKYQlSY4eOhZR3eNJM84130_provenance.
- NP760807.RAYKnN6UefydXt1QTbRIse4QvUocLX62A4xEzJjX3sX2w130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760807.RAYKnN6UefydXt1QTbRIse4QvUocLX62A4xEzJjX3sX2w130_provenance.
- NP760808.RAfMXRGgXUZesCSmFouWEag022u9Fbnqrjm2muj892ffA130_assertion description "[Heterozygous mutations of SHOX have been implicated in patients with Madelung's deformity, Leri-Weill dyschondrosteosis (77%), Turner's syndrome (66%), and idiopathic short stature (3%), and homozygous mutations of SHOX gene have been identified in patients with Langer's mesomelic dysplasia (100%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760808.RAfMXRGgXUZesCSmFouWEag022u9Fbnqrjm2muj892ffA130_provenance.