Chromosomal variation in man: a catalog of chromosomal variants and anomalies
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
New York u.a.
Wiley-Liss
1991
|
| Ausgabe: | 6. ed. |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | LXXVI, 1024 S. Ill. |
| ISBN: | 0471561576 |
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| 245 | 1 | 0 | |a Chromosomal variation in man |b a catalog of chromosomal variants and anomalies |c Digamber S. Borgaonkar |
| 250 | |a 6. ed. | ||
| 264 | 1 | |a New York u.a. |b Wiley-Liss |c 1991 | |
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| 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 | |
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Datensatz im Suchindex
| _version_ | 1804119682710503424 |
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| adam_text | CHROMOSOMAL VARIATION IN MAN A CATALOG OF CHROMOSOMAL VARIANTS AND
ANOMALIES 6TH EDITION DIGAMBER S. BORGAONKAR, PH.D. DIRECTOR,
CYTOGENETICS LABORATORY; DR. MARGARET I. HANDY CHAIR IN HUMAN GENETICS,
MEDICAL CENTER OF DELAWARE; ADJUNCT PROFESSOR, SCHOOL OF LIFE AND HEALTH
SCIENCES, UNIVERSITY OF DELAWARE, NEWARK, DELAWARE; AND RESEARCH
PROFESSOR IN GENETICS, THOMAS JEFFERSON UNIVERSITY, PHILADELPHIA,
PENNSYLVANIA IWILEY-LISS A JOHN WILEY & SONS, INC., PUBLICATION NEW YORK
* CHICHESTER * BRISBANE * TORONTO * SINGAPORE CONTENTS LIST OF TABLES XI
PREFACE XIII REFERENCES XXVII ON THE USE OF THE CATALOG XXIX SOURCES
XXXI ACKNOWLEDGEMENTS*SIXTH EDITION XXXII REPORTS OF CHROMOSOME STUDIES
IN MENDELIAN DISORDERS WITH MCKUSICK CATALOG NUMBERS BY MIM # S XXXIII
REPORTS OF CHROMOSOME STUDIES IN MENDELIAN DISORDERS WITH MCKUSICK
CATALOG NUMBERS BY CHROMOSOME BREAKPOINTS LI MODIFIED ISCN (1985)
IDEOGRAMS IXIX STRUCTURAL VARIATIONS AND ANOMALIES 1 01 1 02 54 03 102
04 . . 146 05 195 06 238 07 270 08 308 09 337 10 383 11 412 12 446 13
467 14 , 511 15 536 16 568 17 582 18 597 19 621 20 627 21 636 22 *: 658
OX 676 0Y 737 VII VIII / CONTENTS 46,XX MALE 763 46,XX OR XY (GONADAL
DYSGENESIS) 766 46,XX OR XY FEMALE (GONADAL AGENESIS) 767 46,XX OR XY
FEMALE (GONADAL DYSGENESIS) 767 46,XY FEMALE 770 MOLES 771 CHIMERA 772
ASYNAPSIS-DESYNAPSIS 774 NUMERICAL ANOMALIES 775 1 ; 775 2 775 3 776 4
777 5 777 6 778 7 778 8 780 9 785 10 788 11 789 12 789 13 790 14 794 15
796 16 797 17 799 18 799 19 806 20 807 21 809 22 827 MAR ., 830 X
CHROMOSOME 837 45,X 837 47,XXX 852 48,XXXX 855 49,XXXXX 856 47,XXY 858
48,XXXY 866 49,XXXXY 866 Y CHROMOSOME , 869 47,XYY 869 48,XYYY 873
49,XYYYY 873 DOUBLE ANEUPLOIDY: ANOMALIES OF MORE THAN ONE AUTOSOME 873
48, + 2, + 16 873 48, + 2, + 9 873 CONTENTS / IX 48, + 5, + 8 873 48, +
8, + 20 874 48, + 8, + 21 874 48, +13, +18 874 48, + 13, + 20 874 48, +
13, + 21 . 874 48, + 16, + 20 874 48, + 16, + 21 874 48, + 18, + 21 874
48, + 21, + 21 874 48, + 21, + MAR 875 49,+6, + 21, + 22 . 875 52, + 2.
+ 7, + 8, + 12, + 13, + 20 875 DOUBLE ANEUPLOIDY: ANOMALIES OF AN
AUTOSOME AND A SEX CHROMOSOME 875 45,X/47,XX, + 21 875 46X + 20 875
46,X, + 21 875 48,XXX, + 7 876 48,XXX, + 18 876 48,XXX, + 21 876
45,X/47,XY, +13 877 45,X/47,XY, +18 877 45,X/46,XY/47,XY, + 21 877
48,XXY, + 8 877 48,XXY, + 13 877 48,XXY, + 16 877 48,XXY, + 18 877
48,XXY, + 21 877 49,XXXY, +18 878 49,XXXY, + 21 878 48,XYY, + 13 878
48,XYY, + 18 878 48,XYY, + 21 879 DOUBLE ANEUPLOIDY: ANOMALIES OF BOTH
THE SEX CHROMOSOMES: X AND Y 879 45,X/47,XYY 879 48.XXYY 879 49.XXXYY
881 49,XXYYY 881 TRIPLE ANEUPLOIDY: ANOMALIES OF BOTH SEX CHROMOSOMES
AND AN AUTOSOME 881 49,XXYY, + 8 881 49,XXYY, +18 881 POLYPLOIDY 882
TRIPLOIDY 882 TETRAPLOIDY 889 X / CONTENTS CHROMOSOMAL BREAKAGE
SYNDROMES . 891 ATAXIA-TELANGIECTASIA (OR LOUIS-BAR SYNDROME) 891 BLOOM
SYNDROME 894 CHROMOSOME INSTABILITY SYNDROME 896 COCKAYNE SYNDROME 896
DYSKERATOSIS CONGENITA 896 FANCONI ANEMIA . 896 INCONTINENTIA PIGMENTI
900 ITAI-LTAI DISEASE 901 MEDULLARY CARCINOMA OF THE THYROID 901
MULTIPLE ENDOCRINE ADENOMATOSIS 901 MULTIPLE SCLEROSIS - 901 NIJMEGEN
SYNDROME 901 PREMATURE CENTROMERE DIVISION 901 ROBERTS SYNDROME 902
ROTHMUND-THOMSON SYNDROME 903 SCLERODERMA 903 SEZARY SYNDROME 904
SHWACHMAN SYNDROME 904 TUBEROUS SCLEROSIS 904 WERNER SYNDROME 904
XERODERMA PIGMENTOSUM 905 INDEX OF AUTHORS 907 INDEX OF SUBJECTS, 1009
|
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| callnumber-first | R - Medicine |
| callnumber-label | RB155 |
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| callnumber-search | RB155.5 |
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| callnumber-subject | RB - Pathology |
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| dewey-search | 616/.042 |
| dewey-sort | 3616 242 |
| dewey-tens | 610 - Medicine and health |
| discipline | Biologie Medizin |
| edition | 6. ed. |
| format | Book |
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| language | English |
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| spelling | Borgaonkar, Digamber S. Verfasser aut Chromosomal variation in man a catalog of chromosomal variants and anomalies Digamber S. Borgaonkar 6. ed. New York u.a. Wiley-Liss 1991 LXXVI, 1024 S. Ill. txt rdacontent n rdamedia nc rdacarrier Afwijkingen gtt Chromosomen gtt Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosom (DE-588)4010162-9 gnd rswk-swf Chromosomenaberration (DE-588)4010163-0 gnd rswk-swf Chromosomenanomalie (DE-588)4122099-7 gnd rswk-swf Mensch (DE-588)4038639-9 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 HEBIS Datenaustausch Mainz application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=003423049&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 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 Afwijkingen gtt Chromosomen gtt Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosom (DE-588)4010162-9 gnd Chromosomenaberration (DE-588)4010163-0 gnd Chromosomenanomalie (DE-588)4122099-7 gnd Mensch (DE-588)4038639-9 gnd |
| subject_GND | (DE-588)4010162-9 (DE-588)4010163-0 (DE-588)4122099-7 (DE-588)4038639-9 (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 Digamber S. Borgaonkar |
| title_fullStr | Chromosomal variation in man a catalog of chromosomal variants and anomalies Digamber S. Borgaonkar |
| title_full_unstemmed | Chromosomal variation in man a catalog of chromosomal variants and anomalies Digamber S. Borgaonkar |
| 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 | Afwijkingen gtt Chromosomen gtt Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosom (DE-588)4010162-9 gnd Chromosomenaberration (DE-588)4010163-0 gnd Chromosomenanomalie (DE-588)4122099-7 gnd Mensch (DE-588)4038639-9 gnd |
| topic_facet | Afwijkingen Chromosomen Chromosome Aberrations Indexes Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Karyotypes Catalogs and collections Chromosom Chromosomenaberration Chromosomenanomalie Mensch Katalog Verzeichnis |
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