Elements of medical genetics (emery's)/ (Record no. 452)

MARC details
000 -LEADER
fixed length control field 02704nam a2200181Ia 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 210804s2007||||xx |||||||||||||| ||und||
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9780702029172
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.042
Item number TUR/EL
100 ## - MAIN ENTRY--AUTHOR NAME
Personal name Turnpenny Peter D
245 #0 - TITLE STATEMENT
Title Elements of medical genetics (emery's)/
250 ## - EDITION STATEMENT
Edition statement 13th
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication Philadelphia:
Name of publisher Churchill livingstone (elsevier),
Year of publication 2007.
300 ## - PHYSICAL DESCRIPTION
Number of Pages 423p.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term principles of human genetics,Gregor Mendel and the laws of inheritance, DNA basis of inheritance,fruit fly,origins of medical genetics, impact of genetic disease, regulation of gene expression , RNA-directed DNA synthesis, mutations, mutagenesis, methods of chromosome analysis, molecular cytogenetics, chromosome nomenclature, gametogenesis, chromosome abnormalities, techniques of DNA analysis, biological hazards of DNA technology, positional cloning, human genome project, developmental genetics, fertilization and gastrulation, hydatidiform moles, epigenetics and development, twinning, patterns of inheritance, Mendelian inheritance, mosaicism, genomic imprinting, mitochondrial inheritance,allele frequencies in populations, genetic polymorphism, segregation analysis, genetic linkage, polygenic and multifactorial inheritance, heritability, hemoglobin and hemoglobinopathies, structure of hemoglobin,developmental expression of hemoglobin, globin chain structure, disorders of hemoglobin, clinical variation of hemoglobinopathies, biochemical genetics, inborn errors of metabolism, urea cycle disorders, disorders of lipid metabolism, organic-acid disorders, peroxisomal disorders, pharmacogenetics, drug metabolism, ecogenetics, immunogenetics, innate immunity, specific acquired immunity, inherited immunodeficiency disorders, cancer genetics, oncogenes, tumor suppressor genes, epigenetics and cancer, genetics of common cancers, genetic counseling in familial cancer, Crohn disease, hemochromatosis, venous thrombosis, atopic diseases, age-related macular degeneration,malformation of unknown cause, genetic counseling, outcomes in genetic counseling, chromosome disorders, chromosomal breakage syndromes, indications for chromosomal analysis, single-gene disorders, Huntington disease,myotonic dystrophy, neurofibromatosis, Marfan syndrome, cystic fibrosis, cardiomyopathies, Duchenne muscular dystrophy,hemophilia, population screening, criteria for screenig program, neonatal screening,genetic registers, prenatal screening, prenatal treatment, risk calculation, autosomal recessive inheritance, autosomal dominant inheritance, Bayes'theorem, empiric risks, gene therapy, ethica dilemmas,ethical and legal issues in medical genetics
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Ellard Sian
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Reference books
Holdings
Withdrawn status Section/Collection code Home library Current library Shelving location Date acquired Source of acquisition(booksellername;invoice_number/date) Subjects/Coded location qualifier Inventory number Full call number Accession Number Koha item type
  MODERN MEDICAL VPSVAC Central Library VPSVAC Central Library REFERENCE 10/07/2009 Purchased GENETICS REF-2-3 616.042 TUR/EL 14521 Reference books
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