Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders:
Gespeichert in:
Hauptverfasser: | , , |
---|---|
Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Erlangen ; Nürnberg
Friedrich-Alexander-Universität Erlangen-Nürnberg
2021
|
Schlagworte: | |
Online-Zugang: | Volltext Volltext |
Beschreibung: | 1 Online-Ressource |
Internformat
MARC
LEADER | 00000nmm a2200000zc 4500 | ||
---|---|---|---|
001 | BV047924319 | ||
003 | DE-604 | ||
005 | 00000000000000.0 | ||
007 | cr|uuu---uuuuu | ||
008 | 220411s2021 gw |||| o||u| ||||||eng d | ||
016 | 7 | |a 1241927421 |2 DE-101 | |
024 | 7 | |a urn:nbn:de:bvb:29-opus4-177339 |2 urn | |
035 | |a (OCoLC)1312703323 | ||
035 | |a (DE-599)DNB1241927421 | ||
040 | |a DE-604 |b ger |e rda | ||
041 | 0 | |8 3\p |a eng | |
044 | |a gw |c XA-DE | ||
049 | |a DE-29 | ||
050 | 0 | |a RB155-155.8 |2 lcc | |
050 | 0 | |a QH431 |2 lcc | |
084 | |8 1\p |a 611.018 |2 23ksdnb | ||
084 | |8 2\p |a 610 |2 23sdnb | ||
100 | 1 | |a Gillentine, Madelyn A. |4 aut | |
245 | 1 | 0 | |a Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders |c Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema [und 95 weitere] |
264 | 1 | |a Erlangen ; Nürnberg |b Friedrich-Alexander-Universität Erlangen-Nürnberg |c 2021 | |
300 | |a 1 Online-Ressource | ||
336 | |b txt |2 rdacontent | ||
337 | |b c |2 rdamedia | ||
338 | |b cr |2 rdacarrier | ||
650 | 0 | |a Cancer research. | |
650 | 0 | |a Human genetics. | |
650 | 0 | |a Medicine. | |
650 | 0 | |a Bioinformatics. | |
650 | 0 | |a Systems biology. | |
650 | 0 | |a Metabolism. | |
653 | |a Human Genetics. | ||
653 | |a Metabolomics. | ||
653 | |a Bioinformatics. | ||
653 | |a Medicine/Public Health, general. | ||
653 | |a Cancer Research. | ||
653 | |a Systems Biology. | ||
700 | 1 | |a Wang, Tianyun |4 aut | |
700 | 1 | |a Hoekzema, Kendra |4 aut | |
787 | 0 | 8 | |i Sonderdruck aus |t Genome Medicine |g Vol. 13 (2021) |o 10.1186/s13073-021-00870-6 |
856 | 4 | 0 | |u https://open.fau.de/handle/openfau/17733 |x Verlag |z kostenfrei |3 Volltext |
856 | 4 | 0 | |u https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-177339 |x Resolving-System |z kostenfrei |3 Volltext |
912 | |a ebook | ||
999 | |a oai:aleph.bib-bvb.de:BVB01-033305909 | ||
883 | 0 | |8 1\p |a aepkn |c 0,87276 |d 20210926 |q DE-101 |u https://d-nb.info/provenance/plan#aepkn | |
883 | 0 | |8 2\p |a aepsg |c 0,99982 |d 20210926 |q DE-101 |u https://d-nb.info/provenance/plan#aepsg | |
883 | 1 | |8 3\p |a npi |d 20210925 |q DE-101 |u https://d-nb.info/provenance/plan#npi |
Datensatz im Suchindex
_version_ | 1804183558833569792 |
---|---|
adam_txt | |
any_adam_object | |
any_adam_object_boolean | |
author | Gillentine, Madelyn A. Wang, Tianyun Hoekzema, Kendra |
author_facet | Gillentine, Madelyn A. Wang, Tianyun Hoekzema, Kendra |
author_role | aut aut aut |
author_sort | Gillentine, Madelyn A. |
author_variant | m a g ma mag t w tw k h kh |
building | Verbundindex |
bvnumber | BV047924319 |
callnumber-first | R - Medicine |
callnumber-label | RB155-155 |
callnumber-raw | RB155-155.8 QH431 |
callnumber-search | RB155-155.8 QH431 |
callnumber-sort | RB 3155 3155.8 |
callnumber-subject | RB - Pathology |
collection | ebook |
ctrlnum | (OCoLC)1312703323 (DE-599)DNB1241927421 |
format | Electronic eBook |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02121nmm a2200577zc 4500</leader><controlfield tag="001">BV047924319</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">220411s2021 gw |||| o||u| ||||||eng d</controlfield><datafield tag="016" ind1="7" ind2=" "><subfield code="a">1241927421</subfield><subfield code="2">DE-101</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">urn:nbn:de:bvb:29-opus4-177339</subfield><subfield code="2">urn</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1312703323</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DNB1241927421</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="8">3\p</subfield><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">XA-DE</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-29</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RB155-155.8</subfield><subfield code="2">lcc</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QH431</subfield><subfield code="2">lcc</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="8">1\p</subfield><subfield code="a">611.018</subfield><subfield code="2">23ksdnb</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="8">2\p</subfield><subfield code="a">610</subfield><subfield code="2">23sdnb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Gillentine, Madelyn A.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders</subfield><subfield code="c">Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema [und 95 weitere]</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Erlangen ; Nürnberg</subfield><subfield code="b">Friedrich-Alexander-Universität Erlangen-Nürnberg</subfield><subfield code="c">2021</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Cancer research.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Human genetics.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Medicine.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Bioinformatics.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Systems biology.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Metabolism.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Human Genetics.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Metabolomics.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Bioinformatics.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Medicine/Public Health, general.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Cancer Research.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Systems Biology.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wang, Tianyun</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hoekzema, Kendra</subfield><subfield code="4">aut</subfield></datafield><datafield tag="787" ind1="0" ind2="8"><subfield code="i">Sonderdruck aus</subfield><subfield code="t">Genome Medicine</subfield><subfield code="g">Vol. 13 (2021)</subfield><subfield code="o">10.1186/s13073-021-00870-6</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://open.fau.de/handle/openfau/17733</subfield><subfield code="x">Verlag</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-177339</subfield><subfield code="x">Resolving-System</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ebook</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-033305909</subfield></datafield><datafield tag="883" ind1="0" ind2=" "><subfield code="8">1\p</subfield><subfield code="a">aepkn</subfield><subfield code="c">0,87276</subfield><subfield code="d">20210926</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#aepkn</subfield></datafield><datafield tag="883" ind1="0" ind2=" "><subfield code="8">2\p</subfield><subfield code="a">aepsg</subfield><subfield code="c">0,99982</subfield><subfield code="d">20210926</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#aepsg</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">3\p</subfield><subfield code="a">npi</subfield><subfield code="d">20210925</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#npi</subfield></datafield></record></collection> |
id | DE-604.BV047924319 |
illustrated | Not Illustrated |
index_date | 2024-07-03T19:33:57Z |
indexdate | 2024-07-10T09:25:22Z |
institution | BVB |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-033305909 |
oclc_num | 1312703323 |
open_access_boolean | 1 |
owner | DE-29 |
owner_facet | DE-29 |
physical | 1 Online-Ressource |
psigel | ebook |
publishDate | 2021 |
publishDateSearch | 2021 |
publishDateSort | 2021 |
publisher | Friedrich-Alexander-Universität Erlangen-Nürnberg |
record_format | marc |
spelling | Gillentine, Madelyn A. aut Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema [und 95 weitere] Erlangen ; Nürnberg Friedrich-Alexander-Universität Erlangen-Nürnberg 2021 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Cancer research. Human genetics. Medicine. Bioinformatics. Systems biology. Metabolism. Human Genetics. Metabolomics. Medicine/Public Health, general. Cancer Research. Systems Biology. Wang, Tianyun aut Hoekzema, Kendra aut Sonderdruck aus Genome Medicine Vol. 13 (2021) 10.1186/s13073-021-00870-6 https://open.fau.de/handle/openfau/17733 Verlag kostenfrei Volltext https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-177339 Resolving-System kostenfrei Volltext 1\p aepkn 0,87276 20210926 DE-101 https://d-nb.info/provenance/plan#aepkn 2\p aepsg 0,99982 20210926 DE-101 https://d-nb.info/provenance/plan#aepsg 3\p npi 20210925 DE-101 https://d-nb.info/provenance/plan#npi |
spellingShingle | Gillentine, Madelyn A. Wang, Tianyun Hoekzema, Kendra Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders Cancer research. Human genetics. Medicine. Bioinformatics. Systems biology. Metabolism. |
title | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders |
title_auth | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders |
title_exact_search | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders |
title_exact_search_txtP | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders |
title_full | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema [und 95 weitere] |
title_fullStr | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema [und 95 weitere] |
title_full_unstemmed | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema [und 95 weitere] |
title_short | Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders |
title_sort | rare deleterious mutations of hnrnp genes result in shared neurodevelopmental disorders |
topic | Cancer research. Human genetics. Medicine. Bioinformatics. Systems biology. Metabolism. |
topic_facet | Cancer research. Human genetics. Medicine. Bioinformatics. Systems biology. Metabolism. |
url | https://open.fau.de/handle/openfau/17733 https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-177339 |
work_keys_str_mv | AT gillentinemadelyna raredeleteriousmutationsofhnrnpgenesresultinsharedneurodevelopmentaldisorders AT wangtianyun raredeleteriousmutationsofhnrnpgenesresultinsharedneurodevelopmentaldisorders AT hoekzemakendra raredeleteriousmutationsofhnrnpgenesresultinsharedneurodevelopmentaldisorders |