Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan
Gespeichert in:
| Veröffentlicht in: | Acta haematologica 2005-01, Vol.114 (2), p.125-126 |
|---|---|
| Hauptverfasser: | , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 126 |
|---|---|
| container_issue | 2 |
| container_start_page | 125 |
| container_title | Acta haematologica |
| container_volume | 114 |
| creator | Karadsheh, Naif S. Gelbart, Terri Schulten, Hans-Jurgen Efferth, Thomas Awidi, Abdalla |
| description | |
| doi_str_mv | 10.1159/000086589 |
| format | Article |
| fullrecord | <record><control><sourceid>pubmed_karge</sourceid><recordid>TN_cdi_karger_primary_86589</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16103639</sourcerecordid><originalsourceid>FETCH-LOGICAL-c303t-5f7ff701f61059e77d1132c3c1ff0d48dcea0fc6b8dd50019ffc289d3370ba8c3</originalsourceid><addsrcrecordid>eNpFkE1PAjEQhhujEUQPnk1Mrx5W2y370aMBRQ1EYtDrpttOobp0SbtI-Av-aotLcC6TmXnemcyL0CUlt5Qm_I6EyNMk50eoS_sxjXiaxseoG9o0SjIed9CZ95-hijPGT1GHppSwlPEu-nmDSjSmtn5hVriEZgNg8aSuQK4r4fCHcEbYxmNhFR5UxhopKjwR1mjwfzpsLJ5toPoGPKrWsvYQpdF0UfvVQjSAh7DYKlfPwYowGYI20oBt8DRchd3iIH-pnRL2HJ1oUXm42Oceen98mA2eovHr6HlwP44kI6yJEp1pnRGqww8JhyxTlLJYMkm1JqqfKwmCaJmWuVJJeJlrLeOcK8YyUopcsh66afdKV3vvQBcrZ5bCbQtKip2fxcHPwF637GpdLkH9k3sDA3DVAl_CzcEdgFb-C8jMe9Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan</title><source>Karger Journals</source><source>MEDLINE</source><creator>Karadsheh, Naif S. ; Gelbart, Terri ; Schulten, Hans-Jurgen ; Efferth, Thomas ; Awidi, Abdalla</creator><creatorcontrib>Karadsheh, Naif S. ; Gelbart, Terri ; Schulten, Hans-Jurgen ; Efferth, Thomas ; Awidi, Abdalla</creatorcontrib><identifier>ISSN: 0001-5792</identifier><identifier>EISSN: 1421-9662</identifier><identifier>DOI: 10.1159/000086589</identifier><identifier>PMID: 16103639</identifier><language>eng</language><publisher>Basel, Switzerland</publisher><subject>Anemia - genetics ; Anemia - pathology ; Brief Communication ; Favism - genetics ; Favism - pathology ; Female ; Glucosephosphate Dehydrogenase - genetics ; Humans ; Infant, Newborn ; Jaundice, Neonatal - genetics ; Jaundice, Neonatal - pathology ; Jordan ; Male ; Point Mutation - genetics</subject><ispartof>Acta haematologica, 2005-01, Vol.114 (2), p.125-126</ispartof><rights>2005 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c303t-5f7ff701f61059e77d1132c3c1ff0d48dcea0fc6b8dd50019ffc289d3370ba8c3</citedby><cites>FETCH-LOGICAL-c303t-5f7ff701f61059e77d1132c3c1ff0d48dcea0fc6b8dd50019ffc289d3370ba8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16103639$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karadsheh, Naif S.</creatorcontrib><creatorcontrib>Gelbart, Terri</creatorcontrib><creatorcontrib>Schulten, Hans-Jurgen</creatorcontrib><creatorcontrib>Efferth, Thomas</creatorcontrib><creatorcontrib>Awidi, Abdalla</creatorcontrib><title>Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan</title><title>Acta haematologica</title><addtitle>Acta Haematol</addtitle><subject>Anemia - genetics</subject><subject>Anemia - pathology</subject><subject>Brief Communication</subject><subject>Favism - genetics</subject><subject>Favism - pathology</subject><subject>Female</subject><subject>Glucosephosphate Dehydrogenase - genetics</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Jaundice, Neonatal - genetics</subject><subject>Jaundice, Neonatal - pathology</subject><subject>Jordan</subject><subject>Male</subject><subject>Point Mutation - genetics</subject><issn>0001-5792</issn><issn>1421-9662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1PAjEQhhujEUQPnk1Mrx5W2y370aMBRQ1EYtDrpttOobp0SbtI-Av-aotLcC6TmXnemcyL0CUlt5Qm_I6EyNMk50eoS_sxjXiaxseoG9o0SjIed9CZ95-hijPGT1GHppSwlPEu-nmDSjSmtn5hVriEZgNg8aSuQK4r4fCHcEbYxmNhFR5UxhopKjwR1mjwfzpsLJ5toPoGPKrWsvYQpdF0UfvVQjSAh7DYKlfPwYowGYI20oBt8DRchd3iIH-pnRL2HJ1oUXm42Oceen98mA2eovHr6HlwP44kI6yJEp1pnRGqww8JhyxTlLJYMkm1JqqfKwmCaJmWuVJJeJlrLeOcK8YyUopcsh66afdKV3vvQBcrZ5bCbQtKip2fxcHPwF637GpdLkH9k3sDA3DVAl_CzcEdgFb-C8jMe9Q</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Karadsheh, Naif S.</creator><creator>Gelbart, Terri</creator><creator>Schulten, Hans-Jurgen</creator><creator>Efferth, Thomas</creator><creator>Awidi, Abdalla</creator><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>20050101</creationdate><title>Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan</title><author>Karadsheh, Naif S. ; Gelbart, Terri ; Schulten, Hans-Jurgen ; Efferth, Thomas ; Awidi, Abdalla</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-5f7ff701f61059e77d1132c3c1ff0d48dcea0fc6b8dd50019ffc289d3370ba8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Anemia - genetics</topic><topic>Anemia - pathology</topic><topic>Brief Communication</topic><topic>Favism - genetics</topic><topic>Favism - pathology</topic><topic>Female</topic><topic>Glucosephosphate Dehydrogenase - genetics</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Jaundice, Neonatal - genetics</topic><topic>Jaundice, Neonatal - pathology</topic><topic>Jordan</topic><topic>Male</topic><topic>Point Mutation - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karadsheh, Naif S.</creatorcontrib><creatorcontrib>Gelbart, Terri</creatorcontrib><creatorcontrib>Schulten, Hans-Jurgen</creatorcontrib><creatorcontrib>Efferth, Thomas</creatorcontrib><creatorcontrib>Awidi, Abdalla</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Acta haematologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karadsheh, Naif S.</au><au>Gelbart, Terri</au><au>Schulten, Hans-Jurgen</au><au>Efferth, Thomas</au><au>Awidi, Abdalla</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan</atitle><jtitle>Acta haematologica</jtitle><addtitle>Acta Haematol</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>114</volume><issue>2</issue><spage>125</spage><epage>126</epage><pages>125-126</pages><issn>0001-5792</issn><eissn>1421-9662</eissn><cop>Basel, Switzerland</cop><pmid>16103639</pmid><doi>10.1159/000086589</doi><tpages>2</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0001-5792 |
| ispartof | Acta haematologica, 2005-01, Vol.114 (2), p.125-126 |
| issn | 0001-5792 1421-9662 |
| language | eng |
| recordid | cdi_karger_primary_86589 |
| source | Karger Journals; MEDLINE |
| subjects | Anemia - genetics Anemia - pathology Brief Communication Favism - genetics Favism - pathology Female Glucosephosphate Dehydrogenase - genetics Humans Infant, Newborn Jaundice, Neonatal - genetics Jaundice, Neonatal - pathology Jordan Male Point Mutation - genetics |
| title | Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T10%3A56%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_karge&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Relationship%20between%20Molecular%20Variants%20and%20Clinical%20Manifestions%20in%20Twelve%20Glucose-6-Phosphate%20Dehydrogenase-Deficient%20Patients%20in%20Jordan&rft.jtitle=Acta%20haematologica&rft.au=Karadsheh,%20Naif%20S.&rft.date=2005-01-01&rft.volume=114&rft.issue=2&rft.spage=125&rft.epage=126&rft.pages=125-126&rft.issn=0001-5792&rft.eissn=1421-9662&rft_id=info:doi/10.1159/000086589&rft_dat=%3Cpubmed_karge%3E16103639%3C/pubmed_karge%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/16103639&rfr_iscdi=true |