Matches in Nanopublications for { ?s ?p "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP789402.RAuyVl9ayaF9P-dHos_u2CGW4-ZIwZBNBwW9v_CGvgYOM130_assertion description "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789402.RAuyVl9ayaF9P-dHos_u2CGW4-ZIwZBNBwW9v_CGvgYOM130_provenance.
- NP301498.RAiU45j_z6C4dpt2MbYtFhUKCdQgX7JHaXuf5kp0xBMnY130_assertion description "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301498.RAiU45j_z6C4dpt2MbYtFhUKCdQgX7JHaXuf5kp0xBMnY130_provenance.
- assertion description "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP935156.RAPqlSc3GBfOwD0pFolDMR34kkzbUNochgYo0VBq5TB2E130_assertion description "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935156.RAPqlSc3GBfOwD0pFolDMR34kkzbUNochgYo0VBq5TB2E130_provenance.
- NP721623.RA_g0YXKhy_2vLQFCdJ68fA-vyvm03_L3tp-WwrR1-djM130_assertion description "[The findings demonstrate that mutations in TRPV4 produce a phenotypic spectrum of skeletal dysplasias from the mild autosomal-dominant brachyolmia to SMDK to autosomal-dominant metatropic dysplasia, suggesting that these disorders should be grouped into a new bone dysplasia family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721623.RA_g0YXKhy_2vLQFCdJ68fA-vyvm03_L3tp-WwrR1-djM130_provenance.