Phenotypic variation: exploration and functional genomics
Gespeichert in:
1. Verfasser: | |
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Format: | Buch |
Sprache: | English |
Veröffentlicht: |
New York [u.a.]
Oxford Univ. Press
2011
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Schlagworte: | |
Online-Zugang: | Inhaltsverzeichnis |
Beschreibung: | XII, 240 S. Ill., graph. Darst. 24 cm |
ISBN: | 9780195379631 0195379632 |
Internformat
MARC
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020 | |a 9780195379631 |c (hbk.) £40.00 |9 978-0-19-537963-1 | ||
020 | |a 0195379632 |c (hbk.) £40.00 |9 0-19-537963-2 | ||
035 | |a (OCoLC)730286461 | ||
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245 | 1 | 0 | |a Phenotypic variation |b exploration and functional genomics |c Moyra Smith |
264 | 1 | |a New York [u.a.] |b Oxford Univ. Press |c 2011 | |
300 | |a XII, 240 S. |b Ill., graph. Darst. |c 24 cm | ||
336 | |b txt |2 rdacontent | ||
337 | |b n |2 rdamedia | ||
338 | |b nc |2 rdacarrier | ||
650 | 2 | |a Phenotype | |
650 | 2 | |a Genetic Variation | |
650 | 2 | |a Genomics | |
650 | 2 | |a Congenital Abnormalities |a genetics | |
650 | 2 | |a Nervous System Diseases |a genetics | |
650 | 0 | 7 | |a Genetische Variabilität |0 (DE-588)4264352-1 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Phänotyp |0 (DE-588)4248244-6 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Genomik |0 (DE-588)4776397-8 |2 gnd |9 rswk-swf |
689 | 0 | 0 | |a Phänotyp |0 (DE-588)4248244-6 |D s |
689 | 0 | 1 | |a Genomik |0 (DE-588)4776397-8 |D s |
689 | 0 | |5 DE-604 | |
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689 | 1 | |C b |5 DE-604 | |
856 | 4 | 2 | |m HBZ Datenaustausch |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=024179290&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
943 | 1 | |a oai:aleph.bib-bvb.de:BVB01-024179290 |
Datensatz im Suchindex
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adam_text |
Titel: Phenotypic variation
Autor: Smith, Moyra
Jahr: 2011
CONTENTS
1. Phenotype and Functional Genomics: Introduction, 3
2. Evolution, 16
3. Genomic Architecture and Copy Number Changes, 35
4. Linkage, Association, and Linkage Disequilibrium, 54
5. Regulation of Transcription, Splicing and Translation: Impact of
Perturbation on Phenotype, 68
6. Mitochondria: Genome, Functions, and Phenotype, 94
7. Quality Surveillance, 121
8. Neurodevelopment and Functional Genomics, 139
9. Neurobehavioral Disorders, 162
10. Molecular Analyses of Malformation Syndromes, 181
xii Contents
11. Multiple Pathways including Environmental Factors that Lead to a
Specific Phenotype with Later Onset, 189
12. Epilogue, 197
References, 200
Index, 229 |
any_adam_object | 1 |
author | Smith, Moyra 1939- |
author_GND | (DE-588)136104649 |
author_facet | Smith, Moyra 1939- |
author_role | aut |
author_sort | Smith, Moyra 1939- |
author_variant | m s ms |
building | Verbundindex |
bvnumber | BV039161815 |
classification_rvk | WG 3000 |
ctrlnum | (OCoLC)730286461 (DE-599)HBZHT016769483 |
dewey-full | 576.5/3 |
dewey-hundreds | 500 - Natural sciences and mathematics |
dewey-ones | 576 - Genetics and evolution |
dewey-raw | 576.5/3 |
dewey-search | 576.5/3 |
dewey-sort | 3576.5 13 |
dewey-tens | 570 - Biology |
discipline | Biologie |
format | Book |
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id | DE-604.BV039161815 |
illustrated | Illustrated |
indexdate | 2024-12-06T17:00:44Z |
institution | BVB |
isbn | 9780195379631 0195379632 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-024179290 |
oclc_num | 730286461 |
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owner | DE-355 DE-BY-UBR |
owner_facet | DE-355 DE-BY-UBR |
physical | XII, 240 S. Ill., graph. Darst. 24 cm |
publishDate | 2011 |
publishDateSearch | 2011 |
publishDateSort | 2011 |
publisher | Oxford Univ. Press |
record_format | marc |
spelling | Smith, Moyra 1939- Verfasser (DE-588)136104649 aut Phenotypic variation exploration and functional genomics Moyra Smith New York [u.a.] Oxford Univ. Press 2011 XII, 240 S. Ill., graph. Darst. 24 cm txt rdacontent n rdamedia nc rdacarrier Phenotype Genetic Variation Genomics Congenital Abnormalities genetics Nervous System Diseases genetics Genetische Variabilität (DE-588)4264352-1 gnd rswk-swf Phänotyp (DE-588)4248244-6 gnd rswk-swf Genomik (DE-588)4776397-8 gnd rswk-swf Phänotyp (DE-588)4248244-6 s Genomik (DE-588)4776397-8 s DE-604 Genetische Variabilität (DE-588)4264352-1 s b DE-604 HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=024179290&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
spellingShingle | Smith, Moyra 1939- Phenotypic variation exploration and functional genomics Phenotype Genetic Variation Genomics Congenital Abnormalities genetics Nervous System Diseases genetics Genetische Variabilität (DE-588)4264352-1 gnd Phänotyp (DE-588)4248244-6 gnd Genomik (DE-588)4776397-8 gnd |
subject_GND | (DE-588)4264352-1 (DE-588)4248244-6 (DE-588)4776397-8 |
title | Phenotypic variation exploration and functional genomics |
title_auth | Phenotypic variation exploration and functional genomics |
title_exact_search | Phenotypic variation exploration and functional genomics |
title_full | Phenotypic variation exploration and functional genomics Moyra Smith |
title_fullStr | Phenotypic variation exploration and functional genomics Moyra Smith |
title_full_unstemmed | Phenotypic variation exploration and functional genomics Moyra Smith |
title_short | Phenotypic variation |
title_sort | phenotypic variation exploration and functional genomics |
title_sub | exploration and functional genomics |
topic | Phenotype Genetic Variation Genomics Congenital Abnormalities genetics Nervous System Diseases genetics Genetische Variabilität (DE-588)4264352-1 gnd Phänotyp (DE-588)4248244-6 gnd Genomik (DE-588)4776397-8 gnd |
topic_facet | Phenotype Genetic Variation Genomics Congenital Abnormalities genetics Nervous System Diseases genetics Genetische Variabilität Phänotyp Genomik |
url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=024179290&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
work_keys_str_mv | AT smithmoyra phenotypicvariationexplorationandfunctionalgenomics |