Matches in Nanopublications for { ?s ?p "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- NP346253.RAcsIbMkvmzjdKvd-GR5dOz39LhZUFu-6sma9FlAk3vT4130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346253.RAcsIbMkvmzjdKvd-GR5dOz39LhZUFu-6sma9FlAk3vT4130_provenance.
- NP442122.RA7sGjDmgxOdFiG6fBJxtYDAFdXpPfxGz5zxxlFOcj208130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442122.RA7sGjDmgxOdFiG6fBJxtYDAFdXpPfxGz5zxxlFOcj208130_provenance.
- NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_provenance.
- assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP332859.RAbLgOm-r1OTMEX40Pibhx25Ta_0qDeW08hGNcdzONyhE130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332859.RAbLgOm-r1OTMEX40Pibhx25Ta_0qDeW08hGNcdzONyhE130_provenance.
- NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.