Matches in Nanopublications for { ?s ?p "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP902166.RAhV8HwSZzGdol3gP2UOo7i-X7B3epA-up3VFy7LLLRWs130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902166.RAhV8HwSZzGdol3gP2UOo7i-X7B3epA-up3VFy7LLLRWs130_provenance.
- NP527106.RAB7sH7861jeGWZuLyhtjfDo4vU_jF-NEiall9IRGRups130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527106.RAB7sH7861jeGWZuLyhtjfDo4vU_jF-NEiall9IRGRups130_provenance.
- NP270751.RAq3JLjNghIcnHBUYfFYVrCLaRVc64zkpNVp-cYPuc-hI130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270751.RAq3JLjNghIcnHBUYfFYVrCLaRVc64zkpNVp-cYPuc-hI130_provenance.
- NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_provenance.
- NP839673.RAZOoRdoCWldWCbS1sOSzr-YFxbulF6HFWhUqKIdeKmGA130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839673.RAZOoRdoCWldWCbS1sOSzr-YFxbulF6HFWhUqKIdeKmGA130_provenance.
- NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- NP676676.RA7xjPdq4bps1vTpbPz9As2m8hEkVlBLsyZHX-YSPp1AE130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676676.RA7xjPdq4bps1vTpbPz9As2m8hEkVlBLsyZHX-YSPp1AE130_provenance.
- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_provenance.
- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_provenance.