Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection
An unbalanced translocation, 46,XX,der(5)t(5;11) (p15;q25)mat was ascertained by prenatal diagnosis. The mother previously had a liveborn child with cri du chat syndrome. The subtlety of the chromosome rearrangement in this case illustrates the need for the most detailed cytogenetic investigations i...
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| Veröffentlicht in: | Obstetrics and gynecology (New York. 1953) 1987-09, Vol.70 (3), p.449-452 |
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| container_title | Obstetrics and gynecology (New York. 1953) |
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| creator | Benn, Peter A. Hsu, Lillian Y. F. Verma, Ram S. Alonso, Lita M. Reich, Elsa Wishnick, Marcia |
| description | An unbalanced translocation, 46,XX,der(5)t(5;11) (p15;q25)mat was ascertained by prenatal diagnosis. The mother previously had a liveborn child with cri du chat syndrome. The subtlety of the chromosome rearrangement in this case illustrates the need for the most detailed cytogenetic investigations in cri du chat cases when deletion or translocation are not immediately obvious. (Obstet Gynecol 70:449, 1987) |
| format | Article |
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F. ; Verma, Ram S. ; Alonso, Lita M. ; Reich, Elsa ; Wishnick, Marcia</creator><creatorcontrib>Benn, Peter A. ; Hsu, Lillian Y. F. ; Verma, Ram S. ; Alonso, Lita M. ; Reich, Elsa ; Wishnick, Marcia</creatorcontrib><description>An unbalanced translocation, 46,XX,der(5)t(5;11) (p15;q25)mat was ascertained by prenatal diagnosis. The mother previously had a liveborn child with cri du chat syndrome. The subtlety of the chromosome rearrangement in this case illustrates the need for the most detailed cytogenetic investigations in cri du chat cases when deletion or translocation are not immediately obvious. 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(Obstet Gynecol 70:449, 1987)</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Chromosome Banding - methods</subject><subject>Chromosome Deletion</subject><subject>Chromosomes, Human, Pair 11</subject><subject>Chromosomes, Human, Pair 5</subject><subject>Cri-du-Chat Syndrome - diagnosis</subject><subject>Female</subject><subject>Fetal Diseases - diagnosis</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Karyotyping</subject><subject>Management. Prenatal diagnosis</subject><subject>Medical sciences</subject><subject>Pregnancy</subject><subject>Pregnancy. Fetus. 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Placenta</topic><topic>Prenatal Diagnosis - methods</topic><topic>Translocation, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Benn, Peter A.</creatorcontrib><creatorcontrib>Hsu, Lillian Y. F.</creatorcontrib><creatorcontrib>Verma, Ram S.</creatorcontrib><creatorcontrib>Alonso, Lita M.</creatorcontrib><creatorcontrib>Reich, Elsa</creatorcontrib><creatorcontrib>Wishnick, Marcia</creatorcontrib><collection>Pascal-Francis</collection><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>Benn, Peter A.</au><au>Hsu, Lillian Y. F.</au><au>Verma, Ram S.</au><au>Alonso, Lita M.</au><au>Reich, Elsa</au><au>Wishnick, Marcia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection</atitle><jtitle>Obstetrics and gynecology (New York. 1953)</jtitle><addtitle>Obstet Gynecol</addtitle><date>1987-09</date><risdate>1987</risdate><volume>70</volume><issue>3</issue><spage>449</spage><epage>452</epage><pages>449-452</pages><issn>0029-7844</issn><eissn>1873-233X</eissn><coden>OBGNAS</coden><abstract>An unbalanced translocation, 46,XX,der(5)t(5;11) (p15;q25)mat was ascertained by prenatal diagnosis. The mother previously had a liveborn child with cri du chat syndrome. The subtlety of the chromosome rearrangement in this case illustrates the need for the most detailed cytogenetic investigations in cri du chat cases when deletion or translocation are not immediately obvious. (Obstet Gynecol 70:449, 1987)</abstract><cop>New York, NY</cop><pub>The American College of Obstetricians and Gynecologists</pub><pmid>3627600</pmid><tpages>4</tpages></addata></record> |
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| identifier | ISSN: 0029-7844 |
| ispartof | Obstetrics and gynecology (New York. 1953), 1987-09, Vol.70 (3), p.449-452 |
| issn | 0029-7844 1873-233X |
| language | eng |
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| source | MEDLINE; Journals@Ovid Complete |
| subjects | Adult Biological and medical sciences Chromosome Banding - methods Chromosome Deletion Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 5 Cri-du-Chat Syndrome - diagnosis Female Fetal Diseases - diagnosis Gynecology. Andrology. Obstetrics Humans Karyotyping Management. Prenatal diagnosis Medical sciences Pregnancy Pregnancy. Fetus. Placenta Prenatal Diagnosis - methods Translocation, Genetic |
| title | Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection |
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