Matches in Nanopublications for { ?s ?p "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP365574.RAiUJ8c2Zd6GeD7EMRHlZPQ3Fejd-ly9UvOTPqL-GE5NY130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365574.RAiUJ8c2Zd6GeD7EMRHlZPQ3Fejd-ly9UvOTPqL-GE5NY130_provenance.
- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_provenance.
- NP502447.RAx193Uma_kCrdprWL7TfBha3XwAOVAVmFJxMpccTc658130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502447.RAx193Uma_kCrdprWL7TfBha3XwAOVAVmFJxMpccTc658130_provenance.
- NP463404.RAynKyAHa_VMsKVzgxwdwKhVGESH6I15gUK-4NHfKDytU130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463404.RAynKyAHa_VMsKVzgxwdwKhVGESH6I15gUK-4NHfKDytU130_provenance.
- assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP589660.RA2gu2EPv-Fg5nL4prbdiPQTAQzRC1N5hEw0v5jvcecz8130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589660.RA2gu2EPv-Fg5nL4prbdiPQTAQzRC1N5hEw0v5jvcecz8130_provenance.
- NP589662.RAQSx73zmj_h8iGeuwIbcmwmK0p6MotwQLAoooH9rFw7w130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589662.RAQSx73zmj_h8iGeuwIbcmwmK0p6MotwQLAoooH9rFw7w130_provenance.
- NP463398.RAKRJkrJPh9KLGQnoITN0AGdoNTHqMsvEl3CVEb6B1FEQ130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463398.RAKRJkrJPh9KLGQnoITN0AGdoNTHqMsvEl3CVEb6B1FEQ130_provenance.
- NP589663.RAHWjCjRNkUM5S3xYWpzjfgURLKjAMQZRMoBUnSy1fnW8130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589663.RAHWjCjRNkUM5S3xYWpzjfgURLKjAMQZRMoBUnSy1fnW8130_provenance.
- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_provenance.