Characterization of a de Novo 43-bp Deletion of the Gsα Gene (GNAS1) in Albright Hereditary Osteodystrophy
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| Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 1994-05, Vol.21 (2), p.455-457 |
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| container_end_page | 457 |
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| container_issue | 2 |
| container_start_page | 455 |
| container_title | Genomics (San Diego, Calif.) |
| container_volume | 21 |
| creator | Luttikhuis, Monique E.M.Oude Wilson, Louise C. Leonard, James V. Trembath, Richard C. |
| description | |
| doi_str_mv | 10.1006/geno.1994.1297 |
| format | Article |
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Joint deformations</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Pedigree</subject><subject>Point Mutation</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Pseudohypoparathyroidism - genetics</subject><subject>Sequence Deletion</subject><issn>0888-7543</issn><issn>1089-8646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1uEzEURi0EKqGwZYfkBUKwmOC_8djLKEBaqWoXhbXl2NeNYTIOtlMpfStehGfqjBK6Y3Wv9J376eog9JaSOSVEfr6DIc2p1mJOme6eoRklSjdKCvkczYhSqulawV-iV6X8JIRortgZOlNTIuQM_VpubLauQo4PtsY04BSwxR7wdbpPWPBmvcNfoId_Wd0AXpW_f_AKBsAfV9eLW_oJxwEv-nWOd5uKLyCDj9XmA74pFZI_lJrTbnN4jV4E2xd4c5rn6Me3r9-XF83VzepyubhqHJeqNp76znMlGaMgqeWt6FrPpGROSW2pF0w4CBDGFTSjXEvOQmht11HvIXh-jj4ce3c5_d5DqWYbi4O-twOkfTGd7BgTuh3B-RF0OZWSIZhdjtvxcUOJmeyaya6Z7JrJ7njw7tS8X2_BP-EnnWP-_pTb4mwfsh1cLE-YIKolmoyYOmIwWriPkE1xEQY3asvgqvEp_u-DRzZzla4</recordid><startdate>19940515</startdate><enddate>19940515</enddate><creator>Luttikhuis, Monique E.M.Oude</creator><creator>Wilson, Louise C.</creator><creator>Leonard, James V.</creator><creator>Trembath, Richard C.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19940515</creationdate><title>Characterization of a de Novo 43-bp Deletion of the Gsα Gene (GNAS1) in Albright Hereditary Osteodystrophy</title><author>Luttikhuis, Monique E.M.Oude ; Wilson, Louise C. ; Leonard, James V. ; Trembath, Richard C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-d1d7d386221e61a35475d2662c869a1d424cefefa1de92139632ff5a771ddefd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromosomes, Human, Pair 20</topic><topic>Diseases of the osteoarticular system</topic><topic>DNA Primers</topic><topic>Exons</topic><topic>Female</topic><topic>Gene Rearrangement</topic><topic>GTP-Binding Proteins - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Malformations and congenital and or hereditary diseases involving bones. 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| fulltext | fulltext |
| identifier | ISSN: 0888-7543 |
| ispartof | Genomics (San Diego, Calif.), 1994-05, Vol.21 (2), p.455-457 |
| issn | 0888-7543 1089-8646 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_76722495 |
| source | MEDLINE; Elsevier ScienceDirect Journals Complete |
| subjects | Base Sequence Biological and medical sciences Chromosomes, Human, Pair 20 Diseases of the osteoarticular system DNA Primers Exons Female Gene Rearrangement GTP-Binding Proteins - genetics Humans Male Malformations and congenital and or hereditary diseases involving bones. Joint deformations Medical sciences Molecular Sequence Data Pedigree Point Mutation Polymerase Chain Reaction - methods Pseudohypoparathyroidism - genetics Sequence Deletion |
| title | Characterization of a de Novo 43-bp Deletion of the Gsα Gene (GNAS1) in Albright Hereditary Osteodystrophy |
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