Inherited 13/14 Chromosome Translocation as a Cause of Human Fetal Wastage
Although many early spontaneous human abortions are associated with a chromosome anomaly, few have been found with a chromosome translocation. However, study of one family with an inherited 13/14 translocation and review of reported cases of recurrent abortions suggest that such translocations may b...
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| Veröffentlicht in: | Obstetrics and gynecology (New York. 1953) 1970-04, Vol.35 (4), p.601-607 |
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| container_title | Obstetrics and gynecology (New York. 1953) |
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| creator | SPARKES, ROBERT S. DE CHIERI, PRIMAROSA R. |
| description | Although many early spontaneous human abortions are associated with a chromosome anomaly, few have been found with a chromosome translocation. However, study of one family with an inherited 13/14 translocation and review of reported cases of recurrent abortions suggest that such translocations may be an important cause of fetal wastage in some families. Cytogenetic reasons for this are considered. Gene linkage studies in the present family are compatible with possible localization of the rhesus locus to the translocated chromosome. |
| format | Article |
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However, study of one family with an inherited 13/14 translocation and review of reported cases of recurrent abortions suggest that such translocations may be an important cause of fetal wastage in some families. Cytogenetic reasons for this are considered. Gene linkage studies in the present family are compatible with possible localization of the rhesus locus to the translocated chromosome.</description><identifier>ISSN: 0029-7844</identifier><identifier>EISSN: 1873-233X</identifier><identifier>PMID: 5438152</identifier><language>eng</language><publisher>United States: The American College of Obstetricians and Gynecologists</publisher><subject>Abortion, Spontaneous ; Adult ; Autoradiography ; Chromosome Aberrations ; Chromosomes, Human, 13-15 ; Female ; Fetal Diseases ; Humans ; Karyotyping ; Pedigree ; Pregnancy</subject><ispartof>Obstetrics and gynecology (New York. 1953), 1970-04, Vol.35 (4), p.601-607</ispartof><rights>1970 The American College of Obstetricians and Gynecologists</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5438152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SPARKES, ROBERT S.</creatorcontrib><creatorcontrib>DE CHIERI, PRIMAROSA R.</creatorcontrib><title>Inherited 13/14 Chromosome Translocation as a Cause of Human Fetal Wastage</title><title>Obstetrics and gynecology (New York. 1953)</title><addtitle>Obstet Gynecol</addtitle><description>Although many early spontaneous human abortions are associated with a chromosome anomaly, few have been found with a chromosome translocation. However, study of one family with an inherited 13/14 translocation and review of reported cases of recurrent abortions suggest that such translocations may be an important cause of fetal wastage in some families. Cytogenetic reasons for this are considered. Gene linkage studies in the present family are compatible with possible localization of the rhesus locus to the translocated chromosome.</description><subject>Abortion, Spontaneous</subject><subject>Adult</subject><subject>Autoradiography</subject><subject>Chromosome Aberrations</subject><subject>Chromosomes, Human, 13-15</subject><subject>Female</subject><subject>Fetal Diseases</subject><subject>Humans</subject><subject>Karyotyping</subject><subject>Pedigree</subject><subject>Pregnancy</subject><issn>0029-7844</issn><issn>1873-233X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1970</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotkE1LxDAYhIMo67r6E4ScvAXz3eQoxXVXFrys6K2k7VtbTZs1aRH_vZXd0zDMw8DMGVoykwnChXg_R0tKuSWZkfISXaX0SSll2ooFWigpDFN8iZ63QwuxG6HGTNwzifM2hj6k0APeRzckHyo3dmHALmGHczclwKHBm6l3A17D6Dx-c2l0H3CNLhrnE9ycdIVe14_7fEN2L0_b_GFHDlwxSzSVDUiqlRFVWeqa6sxw0yhJhdJV6ZyBiltrgDEt6ixTHDhY1igLVU1rK1bo7th7iOF7gjQWfZcq8N4NEKZUGKmkpVzN4O0JnMoe6uIQu97F3-I0fs7lMf8JfoSYvvz0A7FowfmxLeazqOaKEmYzSuXsyP9_VvwBZFZkGg</recordid><startdate>197004</startdate><enddate>197004</enddate><creator>SPARKES, ROBERT S.</creator><creator>DE CHIERI, PRIMAROSA R.</creator><general>The American College of Obstetricians and Gynecologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>197004</creationdate><title>Inherited 13/14 Chromosome Translocation as a Cause of Human Fetal Wastage</title><author>SPARKES, ROBERT S. ; DE CHIERI, PRIMAROSA R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2519-604fe406583cbb6d067828f540356cbaa8ec2998e1163d7752e2e91f59ecd0d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1970</creationdate><topic>Abortion, Spontaneous</topic><topic>Adult</topic><topic>Autoradiography</topic><topic>Chromosome Aberrations</topic><topic>Chromosomes, Human, 13-15</topic><topic>Female</topic><topic>Fetal Diseases</topic><topic>Humans</topic><topic>Karyotyping</topic><topic>Pedigree</topic><topic>Pregnancy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SPARKES, ROBERT S.</creatorcontrib><creatorcontrib>DE CHIERI, PRIMAROSA R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Obstetrics and gynecology (New York. 1953)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SPARKES, ROBERT S.</au><au>DE CHIERI, PRIMAROSA R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inherited 13/14 Chromosome Translocation as a Cause of Human Fetal Wastage</atitle><jtitle>Obstetrics and gynecology (New York. 1953)</jtitle><addtitle>Obstet Gynecol</addtitle><date>1970-04</date><risdate>1970</risdate><volume>35</volume><issue>4</issue><spage>601</spage><epage>607</epage><pages>601-607</pages><issn>0029-7844</issn><eissn>1873-233X</eissn><abstract>Although many early spontaneous human abortions are associated with a chromosome anomaly, few have been found with a chromosome translocation. However, study of one family with an inherited 13/14 translocation and review of reported cases of recurrent abortions suggest that such translocations may be an important cause of fetal wastage in some families. Cytogenetic reasons for this are considered. Gene linkage studies in the present family are compatible with possible localization of the rhesus locus to the translocated chromosome.</abstract><cop>United States</cop><pub>The American College of Obstetricians and Gynecologists</pub><pmid>5438152</pmid><tpages>7</tpages></addata></record> |
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| identifier | ISSN: 0029-7844 |
| ispartof | Obstetrics and gynecology (New York. 1953), 1970-04, Vol.35 (4), p.601-607 |
| issn | 0029-7844 1873-233X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_84549025 |
| source | MEDLINE; Journals@Ovid Complete |
| subjects | Abortion, Spontaneous Adult Autoradiography Chromosome Aberrations Chromosomes, Human, 13-15 Female Fetal Diseases Humans Karyotyping Pedigree Pregnancy |
| title | Inherited 13/14 Chromosome Translocation as a Cause of Human Fetal Wastage |
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