Chromosomal variation in man: a catalog of chromosomal variants and anomalies
Over 1500 entries to literature (mostly English-language journal articles). Sources were Current contents, various genetics journals, Excerpta medica, and Index medicus. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosome breakage syndromes...
Saved in:
| Main Author: | |
|---|---|
| Format: | Book |
| Language: | English |
| Published: |
New York
Liss
1977
|
| Edition: | 2. ed. |
| Subjects: | |
| Summary: | Over 1500 entries to literature (mostly English-language journal articles). Sources were Current contents, various genetics journals, Excerpta medica, and Index medicus. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosome breakage syndromes. Author, selected syndrome index. |
| Physical Description: | XLVII, 403 S. |
| ISBN: | 084510201X |
Staff View
MARC
| LEADER | 00000nam a2200000 c 4500 | ||
|---|---|---|---|
| 001 | BV002154930 | ||
| 003 | DE-604 | ||
| 005 | 00000000000000.0 | ||
| 007 | t | ||
| 008 | 890928s1977 |||| 00||| eng d | ||
| 020 | |a 084510201X |9 0-8451-0201-X | ||
| 035 | |a (OCoLC)3396488 | ||
| 035 | |a (DE-599)BVBBV002154930 | ||
| 040 | |a DE-604 |b ger |e rakddb | ||
| 041 | 0 | |a eng | |
| 049 | |a DE-12 |a DE-703 |a DE-29 |a DE-91 | ||
| 050 | 0 | |a RB155 | |
| 082 | 0 | |a 616/.042 | |
| 084 | |a WG 6908 |0 (DE-625)148601: |2 rvk | ||
| 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 |
| 250 | |a 2. ed. | ||
| 264 | 1 | |a New York |b Liss |c 1977 | |
| 300 | |a XLVII, 403 S. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 520 | |a Over 1500 entries to literature (mostly English-language journal articles). Sources were Current contents, various genetics journals, Excerpta medica, and Index medicus. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosome breakage syndromes. Author, selected syndrome index. | ||
| 650 | 4 | |a Caryotypes - Catalogues | |
| 650 | 4 | |a Chromosomes humains - Anomalies - Catalogues | |
| 650 | 4 | |a Chromosomes humains - Catalogues | |
| 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 Chromosomenaberration |0 (DE-588)4010163-0 |2 gnd |9 rswk-swf |
| 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 |
| 655 | 7 | |0 (DE-588)4163417-2 |a Katalog |2 gnd-content | |
| 689 | 0 | 0 | |a Chromosom |0 (DE-588)4010162-9 |D s |
| 689 | 0 | 1 | |a Mensch |0 (DE-588)4038639-9 |D s |
| 689 | 0 | |5 DE-604 | |
| 689 | 1 | 0 | |a Chromosomenanomalie |0 (DE-588)4122099-7 |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:BVB01-001414323 | ||
| 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 | |
| 980 | 4 | |a (DE-12)AK02840110 | |
Record in the Search Index
| _version_ | 1804116610416377856 |
|---|---|
| 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 | BV002154930 |
| callnumber-first | R - Medicine |
| callnumber-label | RB155 |
| callnumber-raw | RB155 |
| callnumber-search | RB155 |
| callnumber-sort | RB 3155 |
| callnumber-subject | RB - Pathology |
| classification_rvk | WG 6908 |
| ctrlnum | (OCoLC)3396488 (DE-599)BVBBV002154930 |
| 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 | Biologie Medizin |
| edition | 2. ed. |
| format | Book |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02400nam a2200577 c 4500</leader><controlfield tag="001">BV002154930</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">890928s1977 |||| 00||| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">084510201X</subfield><subfield code="9">0-8451-0201-X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)3396488</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV002154930</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-12</subfield><subfield code="a">DE-703</subfield><subfield code="a">DE-29</subfield><subfield code="a">DE-91</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="084" ind1=" " ind2=" "><subfield code="a">WG 6908</subfield><subfield code="0">(DE-625)148601:</subfield><subfield code="2">rvk</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="250" ind1=" " ind2=" "><subfield code="a">2. ed.</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">New York</subfield><subfield code="b">Liss</subfield><subfield code="c">1977</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XLVII, 403 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 1500 entries to literature (mostly English-language journal articles). Sources were Current contents, various genetics journals, Excerpta medica, and Index medicus. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosome breakage syndromes. Author, selected syndrome index.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Caryotypes - Catalogues</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains - Anomalies - Catalogues</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains - Catalogues</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">Chromosomenaberration</subfield><subfield code="0">(DE-588)4010163-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</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="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="689" ind1="0" 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="0" 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="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="1" 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="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:BVB01-001414323</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><datafield tag="980" ind1="4" ind2=" "><subfield code="a">(DE-12)AK02840110</subfield></datafield></record></collection> |
| genre | (DE-588)4163417-2 Katalog gnd-content |
| genre_facet | Katalog |
| id | DE-604.BV002154930 |
| illustrated | Not Illustrated |
| indexdate | 2024-07-09T15:41:15Z |
| institution | BVB |
| isbn | 084510201X |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-001414323 |
| oclc_num | 3396488 |
| open_access_boolean | |
| owner | DE-12 DE-703 DE-29 DE-91 DE-BY-TUM |
| owner_facet | DE-12 DE-703 DE-29 DE-91 DE-BY-TUM |
| physical | XLVII, 403 S. |
| publishDate | 1977 |
| publishDateSearch | 1977 |
| publishDateSort | 1977 |
| publisher | Liss |
| record_format | marc |
| spelling | Borgaonkar, Digamber S. Verfasser aut Chromosomal variation in man a catalog of chromosomal variants and anomalies 2. ed. New York Liss 1977 XLVII, 403 S. txt rdacontent n rdamedia nc rdacarrier Over 1500 entries to literature (mostly English-language journal articles). Sources were Current contents, various genetics journals, Excerpta medica, and Index medicus. Entries arranged under sections titled Structural variations and anomalies, Numerical anomalies, and Chromosome breakage syndromes. Author, selected syndrome index. Caryotypes - Catalogues Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Catalogues Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosomenaberration (DE-588)4010163-0 gnd rswk-swf Mensch (DE-588)4038639-9 gnd rswk-swf Chromosom (DE-588)4010162-9 gnd rswk-swf Chromosomenanomalie (DE-588)4122099-7 gnd rswk-swf (DE-588)4163417-2 Katalog gnd-content Chromosom (DE-588)4010162-9 s Mensch (DE-588)4038639-9 s DE-604 Chromosomenanomalie (DE-588)4122099-7 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 Caryotypes - Catalogues Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Catalogues Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosomenaberration (DE-588)4010163-0 gnd Mensch (DE-588)4038639-9 gnd Chromosom (DE-588)4010162-9 gnd Chromosomenanomalie (DE-588)4122099-7 gnd |
| subject_GND | (DE-588)4010163-0 (DE-588)4038639-9 (DE-588)4010162-9 (DE-588)4122099-7 (DE-588)4163417-2 |
| 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 | Caryotypes - Catalogues Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Catalogues Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosomenaberration (DE-588)4010163-0 gnd Mensch (DE-588)4038639-9 gnd Chromosom (DE-588)4010162-9 gnd Chromosomenanomalie (DE-588)4122099-7 gnd |
| topic_facet | Caryotypes - Catalogues Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Catalogues Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosomenaberration Mensch Chromosom Chromosomenanomalie Katalog |
| work_keys_str_mv | AT borgaonkardigambers chromosomalvariationinmanacatalogofchromosomalvariantsandanomalies |