Matches in Nanopublications for { ?s ?p "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_provenance.
- NP606461.RAv7tp1NVtnkfuNRYO5a15psa-_dlw3aagITnaRTw7-tw130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606461.RAv7tp1NVtnkfuNRYO5a15psa-_dlw3aagITnaRTw7-tw130_provenance.
- NP841222.RAcFuoyWx21z-jqAXjuayfVeMvvKMby3yY3_rQF4N28w0130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841222.RAcFuoyWx21z-jqAXjuayfVeMvvKMby3yY3_rQF4N28w0130_provenance.
- assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP282264.RAEQTvpab6F6z49lwoV40KMnXjOOGGvmbFiQeFAI320c4130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282264.RAEQTvpab6F6z49lwoV40KMnXjOOGGvmbFiQeFAI320c4130_provenance.
- assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409251.RAc801iuLBw_0X-CAi5iumt8xz4_KFRDw5W5EraKBEQfI130_provenance.
- NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460537.RAKMMIuBLbBRj1RYuF-p3CDvLyqSYFmhkhCte86ojjIEw130_provenance.
- NP314938.RAeaRaWcumzM4OL__vvgdtYxFN-UIvPUcJgEjVOq0HL48130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314938.RAeaRaWcumzM4OL__vvgdtYxFN-UIvPUcJgEjVOq0HL48130_provenance.
- NP314940.RAULrhi41TP07FA_wEuxA2pAtedmyEdfcuTvGkEf1sDnE130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314940.RAULrhi41TP07FA_wEuxA2pAtedmyEdfcuTvGkEf1sDnE130_provenance.
- NP409268.RAs1SHhNovGnq8Yr8tBe5-c3s1JEY71XtDhQN6iTozs_0130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409268.RAs1SHhNovGnq8Yr8tBe5-c3s1JEY71XtDhQN6iTozs_0130_provenance.
- NP412861.RAHj65hxxOiBcASFl-7J9Ci6kI278x5uqSoX9slHJ0U6w130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412861.RAHj65hxxOiBcASFl-7J9Ci6kI278x5uqSoX9slHJ0U6w130_provenance.
- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_provenance.
- NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314933.RAHstz7ggxWq-Ih1b9Z6c9fJR_8gE0xru6vKXl3FM-JNA130_provenance.
- NP314934.RAO9J_A1JXvFKoMyUw68p0CgZk2bt-tcteyuprOohYyRQ130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314934.RAO9J_A1JXvFKoMyUw68p0CgZk2bt-tcteyuprOohYyRQ130_provenance.