Matches in Nanopublications for { ?s ?p "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP320336.RAKDRBem818cu9VmkKtIE5jJ67o9o_SoodE9PXfLmJlP8130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320336.RAKDRBem818cu9VmkKtIE5jJ67o9o_SoodE9PXfLmJlP8130_provenance.
- NP661232.RA7HacW_RfnwjIcVRLTz-BFdpAO32Gm6ziHR0dwG9Xcsg130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661232.RA7HacW_RfnwjIcVRLTz-BFdpAO32Gm6ziHR0dwG9Xcsg130_provenance.
- NP354973.RAbZrjiuGGngbuhrJdVi2lAMGlBKyCnMptqbzZc68Ca-c130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354973.RAbZrjiuGGngbuhrJdVi2lAMGlBKyCnMptqbzZc68Ca-c130_provenance.
- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_provenance.
- NP360583.RAeULgZWZZZ-Lt-dQ0i-8MTujnk9Sa1Zni4FzhDLlOrv0130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360583.RAeULgZWZZZ-Lt-dQ0i-8MTujnk9Sa1Zni4FzhDLlOrv0130_provenance.
- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_provenance.
- NP360584.RAA6RXDsXD5rZKqrvIxN1W-f6ZK6UwmnnzYPjoKkPkkb4130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360584.RAA6RXDsXD5rZKqrvIxN1W-f6ZK6UwmnnzYPjoKkPkkb4130_provenance.
- NP354986.RAytlSEevH-sQHyMjDfFuk4Jx4WdUle8Yq-g2tWfbWa-s130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354986.RAytlSEevH-sQHyMjDfFuk4Jx4WdUle8Yq-g2tWfbWa-s130_provenance.
- NP354988.RAJR-J1UP6Nf9L1NiKkRgUpMDOEp9EbqBUI1dQkx83PPg130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354988.RAJR-J1UP6Nf9L1NiKkRgUpMDOEp9EbqBUI1dQkx83PPg130_provenance.
- NP355006.RAPDEKLKg7-YLDslPLAMVHOomeIOFaoaMxyfjwCjx9Aag130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355006.RAPDEKLKg7-YLDslPLAMVHOomeIOFaoaMxyfjwCjx9Aag130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355014.RAMbjZRB3zBfyLv1uAxj9doGK2fKdiD4CNlfgz-1nUclo130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355014.RAMbjZRB3zBfyLv1uAxj9doGK2fKdiD4CNlfgz-1nUclo130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_provenance.
- NP360585.RAx8pJT452F8ILtDKpYKANiVDj5oksRrDQIQ4cKrvwFt4130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360585.RAx8pJT452F8ILtDKpYKANiVDj5oksRrDQIQ4cKrvwFt4130_provenance.
- NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.