Congenital Heart Disease Molecular Diagnostics

Recent exciting advances in molecular genetics and in our understanding of the molecular basis for cardiovascular disease have now made it possible to use genetic tests to identify and provide early treatment for those patients at risk for heart disease. In Congenital Heart Disease: Molecular Diagno...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Weitere Verfasser: Kearns-Jonker, Mary (HerausgeberIn)
Format: Elektronisch E-Book
Sprache:English
Veröffentlicht: Totowa, NJ Humana Press 2006
Schriftenreihe:Methods in Molecular Medicine 126
Schlagworte:
Online-Zugang:DE-355
DE-91
URL des Erstveröffentlichers
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

MARC

LEADER 00000nam a2200000zcb4500
001 BV044952401
003 DE-604
005 20180829
007 cr|uuu---uuuuu
008 180517s2006 xx o|||| 00||| eng d
020 |a 9781597450881  |9 978-1-59745-088-1 
024 7 |a 10.1385/159745088X  |2 doi 
035 |a (ZDB-2-PRO)978-1-59745-088-1 
035 |a (OCoLC)890642730 
035 |a (DE-599)BVBBV044952401 
040 |a DE-604  |b ger  |e rda 
041 0 |a eng 
049 |a DE-355  |a DE-91 
050 0 |a RC687 
082 0 |a 616.12  |2 23 
082 0 |a 616.1/042 
084 |a YB 9616  |0 (DE-625)153179:12922  |2 rvk 
245 1 0 |a Congenital Heart Disease  |b Molecular Diagnostics  |c edited by Mary Kearns-Jonker 
264 1 |a Totowa, NJ  |b Humana Press  |c 2006 
300 |a 1 Online-Ressource (X, 278 p) 
336 |b txt  |2 rdacontent 
337 |b c  |2 rdamedia 
338 |b cr  |2 rdacarrier 
490 0 |a Methods in Molecular Medicine  |v 126 
520 |a Recent exciting advances in molecular genetics and in our understanding of the molecular basis for cardiovascular disease have now made it possible to use genetic tests to identify and provide early treatment for those patients at risk for heart disease. In Congenital Heart Disease: Molecular Diagnostics, prominent researchers and clinicians describe in detail the latest laboratory techniques currently used to define the molecular genetic basis for congenital malformations of the heart, cardiomyopathies, cardiac tumors, and arrythmias in human patients. In particular, the methods can be used to identify in clinical samples those genetic mutations responsible for such congenital abnormalities as Marfan syndrome, Williams-Beuren Syndrome, Alagille syndrome, Noonan syndrome, and Friedreich ataxia. The authors also discuss the limitations of identifying patients with congenital heart disease using these techniques during both pre- and postnatal periods. The protocols follow the successful Methods in Molecular Medicine™ series format, each offering step-by-step laboratory instructions, an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, and tips on troubleshooting, experimental design, and avoiding known pitfalls. Comprehensive and highly practical, Congenital Heart Disease: Molecular Diagnostics not only updates the reader with state-of-the-art information about the genetic basis of cardiovascular disease, but also provides the techniques for early diagnosis and treatment of patients afflicted with heart disease 
650 4 |a Medicine & Public Health 
650 4 |a Cardiology 
650 4 |a Medicine 
650 4 |a Cardiology 
650 0 7 |a Molekulare Diagnostik  |0 (DE-588)4589005-5  |2 gnd  |9 rswk-swf 
650 0 7 |a Angeborene Krankheit  |0 (DE-588)4331107-6  |2 gnd  |9 rswk-swf 
650 0 7 |a Herzfehler  |0 (DE-588)4024646-2  |2 gnd  |9 rswk-swf 
689 0 0 |a Herzfehler  |0 (DE-588)4024646-2  |D s 
689 0 1 |a Angeborene Krankheit  |0 (DE-588)4331107-6  |D s 
689 0 2 |a Molekulare Diagnostik  |0 (DE-588)4589005-5  |D s 
689 0 |C b  |5 DE-604 
700 1 |a Kearns-Jonker, Mary  |4 edt 
776 0 8 |i Erscheint auch als  |n Druck-Ausgabe  |z 9781588293756 
856 4 0 |u https://doi.org/10.1385/159745088X  |x Verlag  |z URL des Erstveröffentlichers  |3 Volltext 
912 |a ZDB-2-PRO 
943 1 |a oai:aleph.bib-bvb.de:BVB01-030345156 
966 e |u https://doi.org/10.1385/159745088X  |l DE-355  |p ZDB-2-PRO  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1385/159745088X  |l DE-91  |p ZDB-2-PRO  |x Verlag  |3 Volltext 

Datensatz im Suchindex

DE-BY-TUM_katkey 2642691
DE-BY-UBR_katkey 6025528
_version_ 1822726611241271296
any_adam_object
author2 Kearns-Jonker, Mary
author2_role edt
author2_variant m k j mkj
author_facet Kearns-Jonker, Mary
building Verbundindex
bvnumber BV044952401
callnumber-first R - Medicine
callnumber-label RC687
callnumber-raw RC687
callnumber-search RC687
callnumber-sort RC 3687
callnumber-subject RC - Internal Medicine
classification_rvk YB 9616
collection ZDB-2-PRO
ctrlnum (ZDB-2-PRO)978-1-59745-088-1
(OCoLC)890642730
(DE-599)BVBBV044952401
dewey-full 616.12
616.1/042
dewey-hundreds 600 - Technology (Applied sciences)
dewey-ones 616 - Diseases
dewey-raw 616.12
616.1/042
dewey-search 616.12
616.1/042
dewey-sort 3616.12
dewey-tens 610 - Medicine and health
discipline Medizin
doi_str_mv 10.1385/159745088X
format Electronic
eBook
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>03510nam a2200541zcb4500</leader><controlfield tag="001">BV044952401</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20180829 </controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">180517s2006 xx o|||| 00||| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9781597450881</subfield><subfield code="9">978-1-59745-088-1</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1385/159745088X</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ZDB-2-PRO)978-1-59745-088-1</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)890642730</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV044952401</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="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-355</subfield><subfield code="a">DE-91</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RC687</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">616.12</subfield><subfield code="2">23</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">616.1/042</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">YB 9616</subfield><subfield code="0">(DE-625)153179:12922</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Congenital Heart Disease</subfield><subfield code="b">Molecular Diagnostics</subfield><subfield code="c">edited by Mary Kearns-Jonker</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Totowa, NJ</subfield><subfield code="b">Humana Press</subfield><subfield code="c">2006</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource (X, 278 p)</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="490" ind1="0" ind2=" "><subfield code="a">Methods in Molecular Medicine</subfield><subfield code="v">126</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Recent exciting advances in molecular genetics and in our understanding of the molecular basis for cardiovascular disease have now made it possible to use genetic tests to identify and provide early treatment for those patients at risk for heart disease. In Congenital Heart Disease: Molecular Diagnostics, prominent researchers and clinicians describe in detail the latest laboratory techniques currently used to define the molecular genetic basis for congenital malformations of the heart, cardiomyopathies, cardiac tumors, and arrythmias in human patients. In particular, the methods can be used to identify in clinical samples those genetic mutations responsible for such congenital abnormalities as Marfan syndrome, Williams-Beuren Syndrome, Alagille syndrome, Noonan syndrome, and Friedreich ataxia. The authors also discuss the limitations of identifying patients with congenital heart disease using these techniques during both pre- and postnatal periods. The protocols follow the successful Methods in Molecular Medicine™ series format, each offering step-by-step laboratory instructions, an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, and tips on troubleshooting, experimental design, and avoiding known pitfalls. Comprehensive and highly practical, Congenital Heart Disease: Molecular Diagnostics not only updates the reader with state-of-the-art information about the genetic basis of cardiovascular disease, but also provides the techniques for early diagnosis and treatment of patients afflicted with heart disease</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Medicine &amp; Public Health</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cardiology</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Medicine</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cardiology</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Molekulare Diagnostik</subfield><subfield code="0">(DE-588)4589005-5</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Angeborene Krankheit</subfield><subfield code="0">(DE-588)4331107-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Herzfehler</subfield><subfield code="0">(DE-588)4024646-2</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Herzfehler</subfield><subfield code="0">(DE-588)4024646-2</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Angeborene Krankheit</subfield><subfield code="0">(DE-588)4331107-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="2"><subfield code="a">Molekulare Diagnostik</subfield><subfield code="0">(DE-588)4589005-5</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="C">b</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kearns-Jonker, Mary</subfield><subfield code="4">edt</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druck-Ausgabe</subfield><subfield code="z">9781588293756</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1385/159745088X</subfield><subfield code="x">Verlag</subfield><subfield code="z">URL des Erstveröffentlichers</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-2-PRO</subfield></datafield><datafield tag="943" ind1="1" ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-030345156</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1385/159745088X</subfield><subfield code="l">DE-355</subfield><subfield code="p">ZDB-2-PRO</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1385/159745088X</subfield><subfield code="l">DE-91</subfield><subfield code="p">ZDB-2-PRO</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield></record></collection>
id DE-604.BV044952401
illustrated Not Illustrated
indexdate 2024-12-24T06:25:55Z
institution BVB
isbn 9781597450881
language English
oai_aleph_id oai:aleph.bib-bvb.de:BVB01-030345156
oclc_num 890642730
open_access_boolean
owner DE-355
DE-BY-UBR
DE-91
DE-BY-TUM
owner_facet DE-355
DE-BY-UBR
DE-91
DE-BY-TUM
physical 1 Online-Ressource (X, 278 p)
psigel ZDB-2-PRO
publishDate 2006
publishDateSearch 2006
publishDateSort 2006
publisher Humana Press
record_format marc
series2 Methods in Molecular Medicine
spellingShingle Congenital Heart Disease Molecular Diagnostics
Medicine & Public Health
Cardiology
Medicine
Molekulare Diagnostik (DE-588)4589005-5 gnd
Angeborene Krankheit (DE-588)4331107-6 gnd
Herzfehler (DE-588)4024646-2 gnd
subject_GND (DE-588)4589005-5
(DE-588)4331107-6
(DE-588)4024646-2
title Congenital Heart Disease Molecular Diagnostics
title_auth Congenital Heart Disease Molecular Diagnostics
title_exact_search Congenital Heart Disease Molecular Diagnostics
title_full Congenital Heart Disease Molecular Diagnostics edited by Mary Kearns-Jonker
title_fullStr Congenital Heart Disease Molecular Diagnostics edited by Mary Kearns-Jonker
title_full_unstemmed Congenital Heart Disease Molecular Diagnostics edited by Mary Kearns-Jonker
title_short Congenital Heart Disease
title_sort congenital heart disease molecular diagnostics
title_sub Molecular Diagnostics
topic Medicine & Public Health
Cardiology
Medicine
Molekulare Diagnostik (DE-588)4589005-5 gnd
Angeborene Krankheit (DE-588)4331107-6 gnd
Herzfehler (DE-588)4024646-2 gnd
topic_facet Medicine & Public Health
Cardiology
Medicine
Molekulare Diagnostik
Angeborene Krankheit
Herzfehler
url https://doi.org/10.1385/159745088X
work_keys_str_mv AT kearnsjonkermary congenitalheartdiseasemoleculardiagnostics