Patient with a non-mosaic isodicentric Yp and mild developmental delay

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part A 2005-08, Vol.137A (2), p.223-224
Hauptverfasser:	Neas, Katherine R., Yip, Moh-Ying, James, Con, Kirk, Edwin P.E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Child, Preschool Chromosome Banding Chromosomes, Human, Y - genetics Developmental Disabilities - pathology Humans In Situ Hybridization, Fluorescence Karyotyping Male Sex Chromosome Disorders - genetics Sex Chromosome Disorders - pathology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

container_end_page	224
container_issue	2
container_start_page	223
container_title	American journal of medical genetics. Part A
container_volume	137A
creator	Neas, Katherine R. Yip, Moh-Ying James, Con Kirk, Edwin P.E.
description
doi_str_mv	10.1002/ajmg.a.30740
format	Article
fullrecord	<record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_20920894</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20920894</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3710-634164329a98707c622de1c918886465c3e49f4ad3c91c5d950fe810306088f33</originalsourceid><addsrcrecordid>eNp9kEtPAjEUhRujEUV3rs2sXDnYx3Sms0QiKAFkoSG6aWrb0WLn4XQQ-fcWQdy5uq_vnpwcAM4Q7CAI8ZWY568d0SEwieAeOEKU4jBihOzvekxb4Ni5OYQE0iQ-BC0UQ4YTSI9Afyoao4smWJrmLRBBURZhXjphZGBcqYz0t9oPT1UgChXkxqpA6U9tyyr3J2H9ZMXqBBxkwjp9uq1t8Ni_eejdhqP7wV2vOwolSRAMYxKhOCI4FSlLYCJjjJVGMkWMsTiKqSQ6SrNIKOJ3kqqUwkwz5H17wywjpA0uNrpVXX4stGt4bpzU1opClwvHMUwxZGnkwcsNKOvSuVpnvKpNLuoVR5Cvc-Pr3LjgP7l5_Hyru3jJtfqDt0F5gGyApbF69a8Y7w7Hg1_ZcPNlXKO_dl-ifudxQhLKZ5MBfx5PerPh9ZRPyDdFzYbh</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20920894</pqid></control><display><type>article</type><title>Patient with a non-mosaic isodicentric Yp and mild developmental delay</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Neas, Katherine R. ; Yip, Moh-Ying ; James, Con ; Kirk, Edwin P.E.</creator><creatorcontrib>Neas, Katherine R. ; Yip, Moh-Ying ; James, Con ; Kirk, Edwin P.E.</creatorcontrib><identifier>ISSN: 1552-4825</identifier><identifier>EISSN: 1552-4833</identifier><identifier>DOI: 10.1002/ajmg.a.30740</identifier><identifier>PMID: 16082705</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Child, Preschool ; Chromosome Banding ; Chromosomes, Human, Y - genetics ; Developmental Disabilities - pathology ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Sex Chromosome Disorders - genetics ; Sex Chromosome Disorders - pathology</subject><ispartof>American journal of medical genetics. Part A, 2005-08, Vol.137A (2), p.223-224</ispartof><rights>Copyright © 2005 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3710-634164329a98707c622de1c918886465c3e49f4ad3c91c5d950fe810306088f33</citedby><cites>FETCH-LOGICAL-c3710-634164329a98707c622de1c918886465c3e49f4ad3c91c5d950fe810306088f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fajmg.a.30740$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fajmg.a.30740$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16082705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Neas, Katherine R.</creatorcontrib><creatorcontrib>Yip, Moh-Ying</creatorcontrib><creatorcontrib>James, Con</creatorcontrib><creatorcontrib>Kirk, Edwin P.E.</creatorcontrib><title>Patient with a non-mosaic isodicentric Yp and mild developmental delay</title><title>American journal of medical genetics. Part A</title><addtitle>Am. J. Med. Genet</addtitle><subject>Child, Preschool</subject><subject>Chromosome Banding</subject><subject>Chromosomes, Human, Y - genetics</subject><subject>Developmental Disabilities - pathology</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Karyotyping</subject><subject>Male</subject><subject>Sex Chromosome Disorders - genetics</subject><subject>Sex Chromosome Disorders - pathology</subject><issn>1552-4825</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPAjEUhRujEUV3rs2sXDnYx3Sms0QiKAFkoSG6aWrb0WLn4XQQ-fcWQdy5uq_vnpwcAM4Q7CAI8ZWY568d0SEwieAeOEKU4jBihOzvekxb4Ni5OYQE0iQ-BC0UQ4YTSI9Afyoao4smWJrmLRBBURZhXjphZGBcqYz0t9oPT1UgChXkxqpA6U9tyyr3J2H9ZMXqBBxkwjp9uq1t8Ni_eejdhqP7wV2vOwolSRAMYxKhOCI4FSlLYCJjjJVGMkWMsTiKqSQ6SrNIKOJ3kqqUwkwz5H17wywjpA0uNrpVXX4stGt4bpzU1opClwvHMUwxZGnkwcsNKOvSuVpnvKpNLuoVR5Cvc-Pr3LjgP7l5_Hyru3jJtfqDt0F5gGyApbF69a8Y7w7Hg1_ZcPNlXKO_dl-ifudxQhLKZ5MBfx5PerPh9ZRPyDdFzYbh</recordid><startdate>20050830</startdate><enddate>20050830</enddate><creator>Neas, Katherine R.</creator><creator>Yip, Moh-Ying</creator><creator>James, Con</creator><creator>Kirk, Edwin P.E.</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><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20050830</creationdate><title>Patient with a non-mosaic isodicentric Yp and mild developmental delay</title><author>Neas, Katherine R. ; Yip, Moh-Ying ; James, Con ; Kirk, Edwin P.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3710-634164329a98707c622de1c918886465c3e49f4ad3c91c5d950fe810306088f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Child, Preschool</topic><topic>Chromosome Banding</topic><topic>Chromosomes, Human, Y - genetics</topic><topic>Developmental Disabilities - pathology</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Karyotyping</topic><topic>Male</topic><topic>Sex Chromosome Disorders - genetics</topic><topic>Sex Chromosome Disorders - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neas, Katherine R.</creatorcontrib><creatorcontrib>Yip, Moh-Ying</creatorcontrib><creatorcontrib>James, Con</creatorcontrib><creatorcontrib>Kirk, Edwin P.E.</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><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>American journal of medical genetics. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neas, Katherine R.</au><au>Yip, Moh-Ying</au><au>James, Con</au><au>Kirk, Edwin P.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patient with a non-mosaic isodicentric Yp and mild developmental delay</atitle><jtitle>American journal of medical genetics. Part A</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>2005-08-30</date><risdate>2005</risdate><volume>137A</volume><issue>2</issue><spage>223</spage><epage>224</epage><pages>223-224</pages><issn>1552-4825</issn><eissn>1552-4833</eissn><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16082705</pmid><doi>10.1002/ajmg.a.30740</doi><tpages>2</tpages></addata></record>
fulltext	fulltext
identifier	ISSN: 1552-4825
ispartof	American journal of medical genetics. Part A, 2005-08, Vol.137A (2), p.223-224
issn	1552-4825 1552-4833
language	eng
recordid	cdi_proquest_miscellaneous_20920894
source	MEDLINE; Access via Wiley Online Library
subjects	Child, Preschool Chromosome Banding Chromosomes, Human, Y - genetics Developmental Disabilities - pathology Humans In Situ Hybridization, Fluorescence Karyotyping Male Sex Chromosome Disorders - genetics Sex Chromosome Disorders - pathology
title	Patient with a non-mosaic isodicentric Yp and mild developmental delay
url	https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T10%3A31%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Patient%20with%20a%20non-mosaic%20isodicentric%20Yp%20and%20mild%20developmental%20delay&rft.jtitle=American%20journal%20of%20medical%20genetics.%20Part%20A&rft.au=Neas,%20Katherine%20R.&rft.date=2005-08-30&rft.volume=137A&rft.issue=2&rft.spage=223&rft.epage=224&rft.pages=223-224&rft.issn=1552-4825&rft.eissn=1552-4833&rft_id=info:doi/10.1002/ajmg.a.30740&rft_dat=%3Cproquest_cross%3E20920894%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=20920894&rft_id=info:pmid/16082705&rfr_iscdi=true