Matches in Nanopublications for { ?s ?p "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP429695.RASmibXuTd17YLnFxGwBoJL-J2rekyTHH27Z6PILZTQG8130_assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429695.RASmibXuTd17YLnFxGwBoJL-J2rekyTHH27Z6PILZTQG8130_provenance.
- NP892383.RAcak8j0JvBgmJiAbpheI-B9TUfP-O5icrvADt9gKiEg8130_assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892383.RAcak8j0JvBgmJiAbpheI-B9TUfP-O5icrvADt9gKiEg8130_provenance.
- NP892382.RAuzaDgal-hynlhWePXNOtOdkOy6Zxqngi4l-ZmnzTdAg130_assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892382.RAuzaDgal-hynlhWePXNOtOdkOy6Zxqngi4l-ZmnzTdAg130_provenance.
- NP429924.RA8vrz-xtOxLEDT3jnj_YtJjQqip-ICS3DDOFGEPdB2mE130_assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429924.RA8vrz-xtOxLEDT3jnj_YtJjQqip-ICS3DDOFGEPdB2mE130_provenance.
- NP892379.RAENIbpaJ4Cj1mhbGqxrLDxDlbzo2e9DxRX5-3tuMKeaU130_assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892379.RAENIbpaJ4Cj1mhbGqxrLDxDlbzo2e9DxRX5-3tuMKeaU130_provenance.
- NP892380.RA3hhbFiGZ3WQXGSwRqf5UPzkUeldRjkvOsetaV3dkXSc130_assertion description "[We identified a GNAS mutation in a patient with a severe form of Albright hereditary osteodystrophy and pseudohypoparathyroidism type 1a with phocomelia and performed PGD on embryos derived by in vitro fertilization in order to deliver an unaffected infant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892380.RA3hhbFiGZ3WQXGSwRqf5UPzkUeldRjkvOsetaV3dkXSc130_provenance.