Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs
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Veröffentlicht in: | American journal of medical genetics. Part A 2004-08, Vol.128A (4), p.431-433 |
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container_title | American journal of medical genetics. Part A |
container_volume | 128A |
creator | Shanske, A.L. Hoper, S.A. Krahn, K. Schutte, B.C. |
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doi_str_mv | 10.1002/ajmg.a.30096 |
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Genet</addtitle><subject>Abnormalities, Multiple - genetics</subject><subject>Cleft Lip - genetics</subject><subject>Cleft Palate - genetics</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Face - abnormalities</subject><subject>Female</subject><subject>Genes, Recessive</subject><subject>Humans</subject><subject>Infant, Low Birth Weight</subject><subject>Infant, Newborn</subject><subject>Interferon Regulatory Factors</subject><subject>Male</subject><subject>Mutation</subject><subject>Pterygium - genetics</subject><subject>Siblings</subject><subject>Syndactyly - genetics</subject><subject>Syndrome</subject><subject>Toes - abnormalities</subject><subject>Transcription Factors - genetics</subject><issn>1552-4825</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9PwjAYhhujEURvnk3_AIfdunbrEYkgBpT4IyZcmm9dq0XGyFqC--8Fh3rz9L2H533z5UHoPCTdkJDoCubFWxe6lBDBD1A7ZCwK4pTSw98csRY6cW5OCCUs4ceoFbKIx5GgbTSbrD14Wy4dtks8ehxwnJd4WXqsYO00vobKu1KBC6awAoddvcyrstA7GrCBwi5qvLH-HftNicEYrbzOsbOZO0VHBhZOn-1vB70Mbp77t8H4YTjq98aBokLwIMnShAgWE011bDItOM8zIJRzSgFSk6ZU5VorIUiUAtv-zUMShgZ0xBnEinbQZbOrqtK5Shu5qmwBVS1DIneK5E6RBPmtaItfNPhqnRU6_4P3TrYAbYCNXej63zHZu5sMf2aDpmWd15-_Lag-JE9owuTr_VDS2aCfPCVTyekX2OeBDw</recordid><startdate>20040801</startdate><enddate>20040801</enddate><creator>Shanske, A.L.</creator><creator>Hoper, S.A.</creator><creator>Krahn, K.</creator><creator>Schutte, B.C.</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></search><sort><creationdate>20040801</creationdate><title>Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs</title><author>Shanske, A.L. ; Hoper, S.A. ; Krahn, K. ; Schutte, B.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3996-7b8709540e3e4fbe966dba036633aa8f883cdeec99028a564261011fae265a4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Abnormalities, Multiple - genetics</topic><topic>Cleft Lip - genetics</topic><topic>Cleft Palate - genetics</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Face - abnormalities</topic><topic>Female</topic><topic>Genes, Recessive</topic><topic>Humans</topic><topic>Infant, Low Birth Weight</topic><topic>Infant, Newborn</topic><topic>Interferon Regulatory Factors</topic><topic>Male</topic><topic>Mutation</topic><topic>Pterygium - genetics</topic><topic>Siblings</topic><topic>Syndactyly - genetics</topic><topic>Syndrome</topic><topic>Toes - abnormalities</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shanske, A.L.</creatorcontrib><creatorcontrib>Hoper, S.A.</creatorcontrib><creatorcontrib>Krahn, K.</creatorcontrib><creatorcontrib>Schutte, B.C.</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><jtitle>American journal of medical genetics. 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source | MEDLINE; Access via Wiley Online Library |
subjects | Abnormalities, Multiple - genetics Cleft Lip - genetics Cleft Palate - genetics DNA-Binding Proteins - genetics Face - abnormalities Female Genes, Recessive Humans Infant, Low Birth Weight Infant, Newborn Interferon Regulatory Factors Male Mutation Pterygium - genetics Siblings Syndactyly - genetics Syndrome Toes - abnormalities Transcription Factors - genetics |
title | Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs |
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