A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome
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| Veröffentlicht in: | American journal of medical genetics. Part A 2009-08, Vol.149A (8), p.1842-1845 |
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| container_end_page | 1845 |
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| container_issue | 8 |
| container_start_page | 1842 |
| container_title | American journal of medical genetics. Part A |
| container_volume | 149A |
| creator | Haldeman-Englert, Chad R. Naeem, Taiyabah Geiger, Elizabeth A. Warnock, Ashley Feret, Holly Ciano, Melissa Davidson, Stefanie L. Deardorff, Matthew A. Zackai, Elaine H. Shaikh, Tamim H. |
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| doi_str_mv | 10.1002/ajmg.a.32980 |
| format | Article |
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Genet</addtitle><subject>Abnormalities, Multiple - genetics</subject><subject>Base Pairing - genetics</subject><subject>Chromosome Deletion</subject><subject>Chromosomes, Human, Pair 13 - genetics</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Syndrome</subject><subject>Young Adult</subject><issn>1552-4825</issn><issn>1552-4833</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtPGzEURq0KVGjaHevKK9h0Uj9y7ZlNpShq01bQh0RbiY3l8dwBwzyCPQHy72tIGugGeWFLPvfosz9CDjgbc8bEe3vZno_tWIoiZy_IPgcQ2SSXcmd7FrBHXsV4yZhkoNVLsscLxVla-2Q2pTrn2VVJK2xw8H1H-5pyec3FWFLfUUsXdvDYDfTWDxf0Bw4YIl00y0jjqqtC3-JrslvbJuKbzT4ivz59PJ19zo6_z7_MpseZmxSKZTxFrDnTPLeVSAk0KgZSuFxWtiw0OMZ1WdZOMEAoUKuylg5BKFewWpVOjsiHtXexLFusXAoVbGMWwbc2rExvvfn_pvMX5ry_MUJLBaCT4GgjCP31EuNgWh8dNo3tsF9GoydQ6BxySOThs6TSIIGnXx6Rd2vQhT7GgPU2Dmfmvh9z34-x5qGfhL99-oRHeFNIAuQauPUNrp6VmenXk_k_bbae8nHAu-2UDVcpqdRg_nybG_H756k-Ucqcyb9vzqlA</recordid><startdate>200908</startdate><enddate>200908</enddate><creator>Haldeman-Englert, Chad R.</creator><creator>Naeem, Taiyabah</creator><creator>Geiger, Elizabeth A.</creator><creator>Warnock, Ashley</creator><creator>Feret, Holly</creator><creator>Ciano, Melissa</creator><creator>Davidson, Stefanie L.</creator><creator>Deardorff, Matthew A.</creator><creator>Zackai, Elaine H.</creator><creator>Shaikh, Tamim H.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>200908</creationdate><title>A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome</title><author>Haldeman-Englert, Chad R. ; Naeem, Taiyabah ; Geiger, Elizabeth A. ; Warnock, Ashley ; Feret, Holly ; Ciano, Melissa ; Davidson, Stefanie L. ; Deardorff, Matthew A. ; Zackai, Elaine H. ; Shaikh, Tamim H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4960-1329f10718ad21967e60532c83dab975c017bbfc205e59e76bf3ce526c90f6bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Abnormalities, Multiple - genetics</topic><topic>Base Pairing - genetics</topic><topic>Chromosome Deletion</topic><topic>Chromosomes, Human, Pair 13 - genetics</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Syndrome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haldeman-Englert, Chad R.</creatorcontrib><creatorcontrib>Naeem, Taiyabah</creatorcontrib><creatorcontrib>Geiger, Elizabeth A.</creatorcontrib><creatorcontrib>Warnock, Ashley</creatorcontrib><creatorcontrib>Feret, Holly</creatorcontrib><creatorcontrib>Ciano, Melissa</creatorcontrib><creatorcontrib>Davidson, Stefanie L.</creatorcontrib><creatorcontrib>Deardorff, Matthew A.</creatorcontrib><creatorcontrib>Zackai, Elaine H.</creatorcontrib><creatorcontrib>Shaikh, Tamim H.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of medical genetics. 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| fulltext | fulltext |
| identifier | ISSN: 1552-4825 |
| ispartof | American journal of medical genetics. Part A, 2009-08, Vol.149A (8), p.1842-1845 |
| issn | 1552-4825 1552-4833 1552-4833 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2736557 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | Abnormalities, Multiple - genetics Base Pairing - genetics Chromosome Deletion Chromosomes, Human, Pair 13 - genetics Female Humans Infant Infant, Newborn Male Oligonucleotide Array Sequence Analysis Syndrome Young Adult |
| title | A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome |
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