Matches in Nanopublications for { ?s ?p "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 9 of
9
with 100 items per page.
- assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP708213.RAW69p0xOaxIrhYvE38dhYUqG1iZk83pfG9GSY50BnOH0130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708213.RAW69p0xOaxIrhYvE38dhYUqG1iZk83pfG9GSY50BnOH0130_provenance.
- NP708214.RANcV_eLPOgC1BZ6a_vh1VpcJ18xkQWf6UQapbcNub4GE130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708214.RANcV_eLPOgC1BZ6a_vh1VpcJ18xkQWf6UQapbcNub4GE130_provenance.
- NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- NP724205.RAxHBhADHGYjuonaaJP0PBDijR1kWD04L20VOWcXRO8bU130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724205.RAxHBhADHGYjuonaaJP0PBDijR1kWD04L20VOWcXRO8bU130_provenance.
- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_provenance.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_provenance.