Loading…
CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping
Saved in:
Published in: | Journal of medical genetics 2000, Vol.37 (12), p.E47-E47 |
---|---|
Main Authors: | , , , , , , , |
Format: | Report |
Language: | English |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | E47 |
container_issue | 12 |
container_start_page | E47 |
container_title | Journal of medical genetics |
container_volume | 37 |
creator | Lev, D Nakar, O Bar-Am, I Zudik, A Watemberg, N Finkelstien, S Katzin, N Lerman-Sagie, T |
description | |
format | report |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_72458495</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72458495</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_724584953</originalsourceid><addsrcrecordid>eNqNi81qwkAURgeh0PTnHe5KElBJJpNocVXE6qqL0kV2MiZXHZ3kxrmjkl0fvYH6AF19h49zBiJIVD4b51KpR_HEfIzjJJ0meSB-Fuv3r9USNDOVRntDDZgGNJQHYyu4GX-ACuGTrtRfjmpiqrUFvUXn_nSVj6AYVejCIvJhMZdR2Eo5SebnNI362GPpsYJtB9z26Pr6pF1HvmtNs38RDzttGV_v-yyGH8vvxXrcOjpfkP2mNlyitbpBuvBmKlU2U29Z-m_xF0GOT8k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>report</recordtype><pqid>72458495</pqid></control><display><type>report</type><title>CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping</title><source>Open Access: PubMed Central</source><creator>Lev, D ; Nakar, O ; Bar-Am, I ; Zudik, A ; Watemberg, N ; Finkelstien, S ; Katzin, N ; Lerman-Sagie, T</creator><creatorcontrib>Lev, D ; Nakar, O ; Bar-Am, I ; Zudik, A ; Watemberg, N ; Finkelstien, S ; Katzin, N ; Lerman-Sagie, T</creatorcontrib><identifier>EISSN: 1468-6244</identifier><language>eng</language><ispartof>Journal of medical genetics, 2000, Vol.37 (12), p.E47-E47</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490</link.rule.ids></links><search><creatorcontrib>Lev, D</creatorcontrib><creatorcontrib>Nakar, O</creatorcontrib><creatorcontrib>Bar-Am, I</creatorcontrib><creatorcontrib>Zudik, A</creatorcontrib><creatorcontrib>Watemberg, N</creatorcontrib><creatorcontrib>Finkelstien, S</creatorcontrib><creatorcontrib>Katzin, N</creatorcontrib><creatorcontrib>Lerman-Sagie, T</creatorcontrib><title>CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping</title><title>Journal of medical genetics</title><issn>1468-6244</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2000</creationdate><recordtype>report</recordtype><recordid>eNqNi81qwkAURgeh0PTnHe5KElBJJpNocVXE6qqL0kV2MiZXHZ3kxrmjkl0fvYH6AF19h49zBiJIVD4b51KpR_HEfIzjJJ0meSB-Fuv3r9USNDOVRntDDZgGNJQHYyu4GX-ACuGTrtRfjmpiqrUFvUXn_nSVj6AYVejCIvJhMZdR2Eo5SebnNI362GPpsYJtB9z26Pr6pF1HvmtNs38RDzttGV_v-yyGH8vvxXrcOjpfkP2mNlyitbpBuvBmKlU2U29Z-m_xF0GOT8k</recordid><startdate>20001201</startdate><enddate>20001201</enddate><creator>Lev, D</creator><creator>Nakar, O</creator><creator>Bar-Am, I</creator><creator>Zudik, A</creator><creator>Watemberg, N</creator><creator>Finkelstien, S</creator><creator>Katzin, N</creator><creator>Lerman-Sagie, T</creator><scope>7X8</scope></search><sort><creationdate>20001201</creationdate><title>CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping</title><author>Lev, D ; Nakar, O ; Bar-Am, I ; Zudik, A ; Watemberg, N ; Finkelstien, S ; Katzin, N ; Lerman-Sagie, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_724584953</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2000</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Lev, D</creatorcontrib><creatorcontrib>Nakar, O</creatorcontrib><creatorcontrib>Bar-Am, I</creatorcontrib><creatorcontrib>Zudik, A</creatorcontrib><creatorcontrib>Watemberg, N</creatorcontrib><creatorcontrib>Finkelstien, S</creatorcontrib><creatorcontrib>Katzin, N</creatorcontrib><creatorcontrib>Lerman-Sagie, T</creatorcontrib><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lev, D</au><au>Nakar, O</au><au>Bar-Am, I</au><au>Zudik, A</au><au>Watemberg, N</au><au>Finkelstien, S</au><au>Katzin, N</au><au>Lerman-Sagie, T</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping</atitle><jtitle>Journal of medical genetics</jtitle><date>2000-12-01</date><risdate>2000</risdate><volume>37</volume><issue>12</issue><spage>E47</spage><epage>E47</epage><pages>E47-E47</pages><eissn>1468-6244</eissn></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1468-6244 |
ispartof | Journal of medical genetics, 2000, Vol.37 (12), p.E47-E47 |
issn | 1468-6244 |
language | eng |
recordid | cdi_proquest_miscellaneous_72458495 |
source | Open Access: PubMed Central |
title | CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T11%3A07%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.atitle=CHARGE%20association%20in%20a%20child%20with%20de%20Novo%20chromosomal%20aberration%2046,%20X,der(X)t(X;2)(p22.1;q33)%20detected%20by%20spectral%20karyotyping&rft.jtitle=Journal%20of%20medical%20genetics&rft.au=Lev,%20D&rft.date=2000-12-01&rft.volume=37&rft.issue=12&rft.spage=E47&rft.epage=E47&rft.pages=E47-E47&rft.eissn=1468-6244&rft_id=info:doi/&rft_dat=%3Cproquest%3E72458495%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_miscellaneous_724584953%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=72458495&rft_id=info:pmid/&rfr_iscdi=true |