Genetic disorders, syndromology and prenatal diagnosis:
Gespeichert in:
| Format: | Buch |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
New York
Liss
1982
|
| Schriftenreihe: | Advances in the study of birth defects
5 |
| Schlagworte: | |
| Beschreibung: | IX, 256 S. |
| ISBN: | 0845130021 |
Internformat
MARC
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|---|---|---|---|
| 001 | BV000031973 | ||
| 003 | DE-604 | ||
| 005 | 19980729 | ||
| 007 | t | ||
| 008 | 870612s1982 |||| 00||| eng d | ||
| 020 | |a 0845130021 |9 0-8451-3002-1 | ||
| 035 | |a (OCoLC)8052737 | ||
| 035 | |a (DE-599)BVBBV000031973 | ||
| 040 | |a DE-604 |b ger |e rakddb | ||
| 041 | 0 | |a eng | |
| 049 | |a DE-12 | ||
| 050 | 0 | |a QM691 | |
| 050 | 0 | |a RB155 | |
| 082 | 0 | |a 616/.042 |2 19 | |
| 084 | |a XG 2200 |0 (DE-625)152789:12905 |2 rvk | ||
| 245 | 1 | 0 | |a Genetic disorders, syndromology and prenatal diagnosis |c ed. by T. V. N. Persaud |
| 264 | 1 | |a New York |b Liss |c 1982 | |
| 300 | |a IX, 256 S. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 490 | 1 | |a Advances in the study of birth defects |v 5 | |
| 650 | 4 | |a Chromosomes humains - Anomalies | |
| 650 | 4 | |a Ftus - Malformations - Diagnostic | |
| 650 | 4 | |a Génétique médicale | |
| 650 | 4 | |a Fetus |x Abnormalities |x Diagnosis | |
| 650 | 4 | |a Genetic Diseases, Inborn | |
| 650 | 4 | |a Genetic disorders | |
| 650 | 4 | |a Human chromosome abnormalities | |
| 650 | 4 | |a Medical genetics | |
| 650 | 4 | |a Prenatal Diagnosis | |
| 650 | 0 | 7 | |a Genetik |0 (DE-588)4071711-2 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Humangenetik |0 (DE-588)4072653-8 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Erbkrankheit |0 (DE-588)4015106-2 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Missbildung |0 (DE-588)4039561-3 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Chromosomenanomalie |0 (DE-588)4122099-7 |2 gnd |9 rswk-swf |
| 689 | 0 | 0 | |a Humangenetik |0 (DE-588)4072653-8 |D s |
| 689 | 0 | |5 DE-604 | |
| 689 | 1 | 0 | |a Erbkrankheit |0 (DE-588)4015106-2 |D s |
| 689 | 1 | 1 | |a Chromosomenanomalie |0 (DE-588)4122099-7 |D s |
| 689 | 1 | |5 DE-604 | |
| 689 | 2 | 0 | |a Genetik |0 (DE-588)4071711-2 |D s |
| 689 | 2 | 1 | |a Missbildung |0 (DE-588)4039561-3 |D s |
| 689 | 2 | |8 1\p |5 DE-604 | |
| 700 | 1 | |a Persaud, Trivedi V. N. |d 1940- |e Sonstige |0 (DE-588)120726068 |4 oth | |
| 830 | 0 | |a Advances in the study of birth defects |v 5 |w (DE-604)BV000001111 |9 5 | |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-000005258 | ||
| 883 | 1 | |8 1\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
Datensatz im Suchindex
| _version_ | 1804114486278225920 |
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| any_adam_object | |
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| building | Verbundindex |
| bvnumber | BV000031973 |
| callnumber-first | Q - Science |
| callnumber-label | QM691 |
| callnumber-raw | QM691 RB155 |
| callnumber-search | QM691 RB155 |
| callnumber-sort | QM 3691 |
| callnumber-subject | QM - Human Anatomy |
| classification_rvk | XG 2200 |
| ctrlnum | (OCoLC)8052737 (DE-599)BVBBV000031973 |
| dewey-full | 616/.042 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 616 - Diseases |
| dewey-raw | 616/.042 |
| dewey-search | 616/.042 |
| dewey-sort | 3616 242 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| format | Book |
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| id | DE-604.BV000031973 |
| illustrated | Not Illustrated |
| indexdate | 2024-07-09T15:07:29Z |
| institution | BVB |
| isbn | 0845130021 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-000005258 |
| oclc_num | 8052737 |
| open_access_boolean | |
| owner | DE-12 |
| owner_facet | DE-12 |
| physical | IX, 256 S. |
| publishDate | 1982 |
| publishDateSearch | 1982 |
| publishDateSort | 1982 |
| publisher | Liss |
| record_format | marc |
| series | Advances in the study of birth defects |
| series2 | Advances in the study of birth defects |
| spelling | Genetic disorders, syndromology and prenatal diagnosis ed. by T. V. N. Persaud New York Liss 1982 IX, 256 S. txt rdacontent n rdamedia nc rdacarrier Advances in the study of birth defects 5 Chromosomes humains - Anomalies Ftus - Malformations - Diagnostic Génétique médicale Fetus Abnormalities Diagnosis Genetic Diseases, Inborn Genetic disorders Human chromosome abnormalities Medical genetics Prenatal Diagnosis Genetik (DE-588)4071711-2 gnd rswk-swf Humangenetik (DE-588)4072653-8 gnd rswk-swf Erbkrankheit (DE-588)4015106-2 gnd rswk-swf Missbildung (DE-588)4039561-3 gnd rswk-swf Chromosomenanomalie (DE-588)4122099-7 gnd rswk-swf Humangenetik (DE-588)4072653-8 s DE-604 Erbkrankheit (DE-588)4015106-2 s Chromosomenanomalie (DE-588)4122099-7 s Genetik (DE-588)4071711-2 s Missbildung (DE-588)4039561-3 s 1\p DE-604 Persaud, Trivedi V. N. 1940- Sonstige (DE-588)120726068 oth Advances in the study of birth defects 5 (DE-604)BV000001111 5 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Genetic disorders, syndromology and prenatal diagnosis Advances in the study of birth defects Chromosomes humains - Anomalies Ftus - Malformations - Diagnostic Génétique médicale Fetus Abnormalities Diagnosis Genetic Diseases, Inborn Genetic disorders Human chromosome abnormalities Medical genetics Prenatal Diagnosis Genetik (DE-588)4071711-2 gnd Humangenetik (DE-588)4072653-8 gnd Erbkrankheit (DE-588)4015106-2 gnd Missbildung (DE-588)4039561-3 gnd Chromosomenanomalie (DE-588)4122099-7 gnd |
| subject_GND | (DE-588)4071711-2 (DE-588)4072653-8 (DE-588)4015106-2 (DE-588)4039561-3 (DE-588)4122099-7 |
| title | Genetic disorders, syndromology and prenatal diagnosis |
| title_auth | Genetic disorders, syndromology and prenatal diagnosis |
| title_exact_search | Genetic disorders, syndromology and prenatal diagnosis |
| title_full | Genetic disorders, syndromology and prenatal diagnosis ed. by T. V. N. Persaud |
| title_fullStr | Genetic disorders, syndromology and prenatal diagnosis ed. by T. V. N. Persaud |
| title_full_unstemmed | Genetic disorders, syndromology and prenatal diagnosis ed. by T. V. N. Persaud |
| title_short | Genetic disorders, syndromology and prenatal diagnosis |
| title_sort | genetic disorders syndromology and prenatal diagnosis |
| topic | Chromosomes humains - Anomalies Ftus - Malformations - Diagnostic Génétique médicale Fetus Abnormalities Diagnosis Genetic Diseases, Inborn Genetic disorders Human chromosome abnormalities Medical genetics Prenatal Diagnosis Genetik (DE-588)4071711-2 gnd Humangenetik (DE-588)4072653-8 gnd Erbkrankheit (DE-588)4015106-2 gnd Missbildung (DE-588)4039561-3 gnd Chromosomenanomalie (DE-588)4122099-7 gnd |
| topic_facet | Chromosomes humains - Anomalies Ftus - Malformations - Diagnostic Génétique médicale Fetus Abnormalities Diagnosis Genetic Diseases, Inborn Genetic disorders Human chromosome abnormalities Medical genetics Prenatal Diagnosis Genetik Humangenetik Erbkrankheit Missbildung Chromosomenanomalie |
| volume_link | (DE-604)BV000001111 |
| work_keys_str_mv | AT persaudtrivedivn geneticdisorderssyndromologyandprenataldiagnosis |