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what is biochemical characteristicsin the last section we have learnt about the importance of biochemical tests it must be clear now that biochemical
explain the importance of biochemical testsspecific series of biochemical tests have been developed for fast identification of microorganisms in
q show the paleobotanical evidencepaleobotany deals with the study of fossil records of plants and animals new techniques and approaches to the study
q explain cytological evidencecytology is the study of the morphology and physiology of cells the information about the chromosome number shape and
q show the anatomical evidenceanatomy is the study of the structure organisation and development of cells and tissues of plants and animals for over
q show the natural selection of taxonomistnatural selection associated with successful reproduction maintains a basic similarity of the reproductive
does every gene mutation cause alteration in the protein the gene normally codifiesnot each gene mutation causes alteration in the composition of the
what are genetic mutationsthe genetic mutations are alterations of the genetic material compared to the normal condition of the species involving
how are genetic diseases classifiedthe genetic diseases classify into chromosomal abnormalities and genetic mutationsbetween chromosomal
do all genetic diseases result from alteration in the number of chromosomes of the cellsbesides aneuploidies there are other genetic diseases other
in general what is the cause of the aneuploidiesin general the aneuploidies are caused by impaired assortment of chromosomes during meiosis for
what is aneuploidy what are the conditions caused by the aneuploidiesthe aneuploidy is an abnormal number of chromosomes in the cells of an
what is the karyotype found in down syndromedown syndrome is the aneuploidy that is a numeric alteration of chromosomes within the cells compared to
why in the preparation of a karyotype analysis is the use of a substance like colchicine interestingthe colchicine is a substance that disallows the
which type of genetic disease can be identified from the visual analysis of the number of chromosomes present in a karyotypethe counting and the
what is karyotypename the karyotype is given to the set of chromosomes of an individual generally when visualized and identified under the microscope
what is the mn blood system what is the pattern of genetic inheritance of the mn blood systema mn blood system is a third in addition to the abo and
how can the hemolytic disease of the newborn be preventedthe erythroblastosis fetalis can be prevented if in the first delivery of a rh child from a
how does the immune process that causes the hemolytic disease of the newborn take placein a hemolytic disease of the newborn the mother has rh- blood
what is the rh typing of the mother and of the fetus in the hemolytic disease of the newbornin a hemolytic disease of the newborn the mother is rh-
what is the logic of the transfusional compatibility concerning the rh blood group systemthe rh donor can only donate blood to the rh recipient the
what are the inheritance and dominance patterns of the rh blood systeman inheritance pattern of the rh blood system is autosomal dominant that is the
how is the blood typing concerning the abo system and the rh usually donein a blood typing for the abo system and the rh system a blood sample is
what is blood typingthe blood typing is the determination by means of tests of the classification of a blood sample concerning blood group systems
how are the antibodies against the rh factor formedthe anti-rh antibodies are made by humoral immune response when the rh- individual makes contact