Chromosomal variation in man: a catalog of chromosomal variants and anomalies
Over 1200 entries to literature (mostly English-language journal articles). Intended for human cytogeneticists. Sources were Current contents, various genetics journals from 1970 to the present, and Excerpta medica and Index medicus for afew earlier references. Entries arranged under sections titled...
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Baltimore u.a.
Johns Hopkins Univ. Pr.
1975
|
| Schlagworte: | |
| Zusammenfassung: | Over 1200 entries to literature (mostly English-language journal articles). Intended for human cytogeneticists. Sources were Current contents, various genetics journals from 1970 to the present, and Excerpta medica and Index medicus for afew earlier references. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosomal breakage syndromes. Author, selected syndrome indexes. |
| Beschreibung: | XVII, 230 S. |
| ISBN: | 0801817196 |
Internformat
MARC
| LEADER | 00000nam a2200000 c 4500 | ||
|---|---|---|---|
| 001 | BV009207151 | ||
| 003 | DE-604 | ||
| 005 | 00000000000000.0 | ||
| 007 | t | ||
| 008 | 940313s1975 |||| 00||| eng d | ||
| 020 | |a 0801817196 |9 0-8018-1719-6 | ||
| 035 | |a (OCoLC)1339599 | ||
| 035 | |a (DE-599)BVBBV009207151 | ||
| 040 | |a DE-604 |b ger |e rakddb | ||
| 041 | 0 | |a eng | |
| 049 | |a DE-29 |a DE-188 | ||
| 050 | 0 | |a RB155 | |
| 082 | 0 | |a 616/.042 | |
| 100 | 1 | |a Borgaonkar, Digamber S. |e Verfasser |4 aut | |
| 245 | 1 | 0 | |a Chromosomal variation in man |b a catalog of chromosomal variants and anomalies |
| 264 | 1 | |a Baltimore u.a. |b Johns Hopkins Univ. Pr. |c 1975 | |
| 300 | |a XVII, 230 S. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 520 | |a Over 1200 entries to literature (mostly English-language journal articles). Intended for human cytogeneticists. Sources were Current contents, various genetics journals from 1970 to the present, and Excerpta medica and Index medicus for afew earlier references. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosomal breakage syndromes. Author, selected syndrome indexes. | ||
| 650 | 4 | |a Chromosomes humains | |
| 650 | 4 | |a Chromosomes humains - Anomalies | |
| 650 | 4 | |a Chromosome Aberrations |v Indexes | |
| 650 | 4 | |a Human chromosome abnormalities |v Catalogs and collections | |
| 650 | 4 | |a Human chromosomes |v Catalogs and collections | |
| 650 | 4 | |a Karyotypes |v Catalogs and collections | |
| 650 | 0 | 7 | |a Mensch |0 (DE-588)4038639-9 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Chromosom |0 (DE-588)4010162-9 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Chromosomenanomalie |0 (DE-588)4122099-7 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Chromosomenaberration |0 (DE-588)4010163-0 |2 gnd |9 rswk-swf |
| 655 | 7 | |0 (DE-588)4163417-2 |a Katalog |2 gnd-content | |
| 655 | 7 | |0 (DE-588)4188171-0 |a Verzeichnis |2 gnd-content | |
| 689 | 0 | 0 | |a Chromosomenanomalie |0 (DE-588)4122099-7 |D s |
| 689 | 0 | |5 DE-604 | |
| 689 | 1 | 0 | |a Chromosom |0 (DE-588)4010162-9 |D s |
| 689 | 1 | 1 | |a Mensch |0 (DE-588)4038639-9 |D s |
| 689 | 1 | |8 1\p |5 DE-604 | |
| 689 | 2 | 0 | |a Chromosomenaberration |0 (DE-588)4010163-0 |D s |
| 689 | 2 | |8 2\p |5 DE-604 | |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-006118615 | ||
| 883 | 1 | |8 1\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
| 883 | 1 | |8 2\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
Datensatz im Suchindex
| _version_ | 1804123646660182016 |
|---|---|
| any_adam_object | |
| author | Borgaonkar, Digamber S. |
| author_facet | Borgaonkar, Digamber S. |
| author_role | aut |
| author_sort | Borgaonkar, Digamber S. |
| author_variant | d s b ds dsb |
| building | Verbundindex |
| bvnumber | BV009207151 |
| callnumber-first | R - Medicine |
| callnumber-label | RB155 |
| callnumber-raw | RB155 |
| callnumber-search | RB155 |
| callnumber-sort | RB 3155 |
| callnumber-subject | RB - Pathology |
| ctrlnum | (OCoLC)1339599 (DE-599)BVBBV009207151 |
| 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 |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02396nam a2200541 c 4500</leader><controlfield tag="001">BV009207151</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">940313s1975 |||| 00||| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0801817196</subfield><subfield code="9">0-8018-1719-6</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1339599</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV009207151</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakddb</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-29</subfield><subfield code="a">DE-188</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RB155</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">616/.042</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Borgaonkar, Digamber S.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Chromosomal variation in man</subfield><subfield code="b">a catalog of chromosomal variants and anomalies</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Baltimore u.a.</subfield><subfield code="b">Johns Hopkins Univ. Pr.</subfield><subfield code="c">1975</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XVII, 230 S.</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">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Over 1200 entries to literature (mostly English-language journal articles). Intended for human cytogeneticists. Sources were Current contents, various genetics journals from 1970 to the present, and Excerpta medica and Index medicus for afew earlier references. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosomal breakage syndromes. Author, selected syndrome indexes.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains - Anomalies</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosome Aberrations</subfield><subfield code="v">Indexes</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Human chromosome abnormalities</subfield><subfield code="v">Catalogs and collections</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Human chromosomes</subfield><subfield code="v">Catalogs and collections</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Karyotypes</subfield><subfield code="v">Catalogs and collections</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Mensch</subfield><subfield code="0">(DE-588)4038639-9</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Chromosom</subfield><subfield code="0">(DE-588)4010162-9</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Chromosomenanomalie</subfield><subfield code="0">(DE-588)4122099-7</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Chromosomenaberration</subfield><subfield code="0">(DE-588)4010163-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)4163417-2</subfield><subfield code="a">Katalog</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)4188171-0</subfield><subfield code="a">Verzeichnis</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Chromosomenanomalie</subfield><subfield code="0">(DE-588)4122099-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="1" ind2="0"><subfield code="a">Chromosom</subfield><subfield code="0">(DE-588)4010162-9</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="1"><subfield code="a">Mensch</subfield><subfield code="0">(DE-588)4038639-9</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2=" "><subfield code="8">1\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="2" ind2="0"><subfield code="a">Chromosomenaberration</subfield><subfield code="0">(DE-588)4010163-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="2" ind2=" "><subfield code="8">2\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-006118615</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">1\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">2\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield></record></collection> |
| genre | (DE-588)4163417-2 Katalog gnd-content (DE-588)4188171-0 Verzeichnis gnd-content |
| genre_facet | Katalog Verzeichnis |
| id | DE-604.BV009207151 |
| illustrated | Not Illustrated |
| indexdate | 2024-07-09T17:33:05Z |
| institution | BVB |
| isbn | 0801817196 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-006118615 |
| oclc_num | 1339599 |
| open_access_boolean | |
| owner | DE-29 DE-188 |
| owner_facet | DE-29 DE-188 |
| physical | XVII, 230 S. |
| publishDate | 1975 |
| publishDateSearch | 1975 |
| publishDateSort | 1975 |
| publisher | Johns Hopkins Univ. Pr. |
| record_format | marc |
| spelling | Borgaonkar, Digamber S. Verfasser aut Chromosomal variation in man a catalog of chromosomal variants and anomalies Baltimore u.a. Johns Hopkins Univ. Pr. 1975 XVII, 230 S. txt rdacontent n rdamedia nc rdacarrier Over 1200 entries to literature (mostly English-language journal articles). Intended for human cytogeneticists. Sources were Current contents, various genetics journals from 1970 to the present, and Excerpta medica and Index medicus for afew earlier references. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosomal breakage syndromes. Author, selected syndrome indexes. Chromosomes humains Chromosomes humains - Anomalies Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Mensch (DE-588)4038639-9 gnd rswk-swf Chromosom (DE-588)4010162-9 gnd rswk-swf Chromosomenanomalie (DE-588)4122099-7 gnd rswk-swf Chromosomenaberration (DE-588)4010163-0 gnd rswk-swf (DE-588)4163417-2 Katalog gnd-content (DE-588)4188171-0 Verzeichnis gnd-content Chromosomenanomalie (DE-588)4122099-7 s DE-604 Chromosom (DE-588)4010162-9 s Mensch (DE-588)4038639-9 s 1\p DE-604 Chromosomenaberration (DE-588)4010163-0 s 2\p DE-604 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 2\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Borgaonkar, Digamber S. Chromosomal variation in man a catalog of chromosomal variants and anomalies Chromosomes humains Chromosomes humains - Anomalies Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Mensch (DE-588)4038639-9 gnd Chromosom (DE-588)4010162-9 gnd Chromosomenanomalie (DE-588)4122099-7 gnd Chromosomenaberration (DE-588)4010163-0 gnd |
| subject_GND | (DE-588)4038639-9 (DE-588)4010162-9 (DE-588)4122099-7 (DE-588)4010163-0 (DE-588)4163417-2 (DE-588)4188171-0 |
| title | Chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_auth | Chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_exact_search | Chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_full | Chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_fullStr | Chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_full_unstemmed | Chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_short | Chromosomal variation in man |
| title_sort | chromosomal variation in man a catalog of chromosomal variants and anomalies |
| title_sub | a catalog of chromosomal variants and anomalies |
| topic | Chromosomes humains Chromosomes humains - Anomalies Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Mensch (DE-588)4038639-9 gnd Chromosom (DE-588)4010162-9 gnd Chromosomenanomalie (DE-588)4122099-7 gnd Chromosomenaberration (DE-588)4010163-0 gnd |
| topic_facet | Chromosomes humains Chromosomes humains - Anomalies Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Mensch Chromosom Chromosomenanomalie Chromosomenaberration Katalog Verzeichnis |
| work_keys_str_mv | AT borgaonkardigambers chromosomalvariationinmanacatalogofchromosomalvariantsandanomalies |