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what is the rh factorthe rh factor is a protein of the red blood cell plasma membrane that behaves as antigen in blood transfusions triggering a
is abo blood compatibility enough for the safety of blood transfusionmoreover abo blood compatibility the compatibility concerning the rh blood
is it possible to perform investigation of natural paternity maternity or brotherhood and sisterhood using the abo blood typingby using an abo blood
what are the genotypes and respective blood types of the abo systemever since the alleles are ia ib and i the possible genotypes are iaia blood type
what is the type of genetic inheritance that determines the abo blood group system what are the relations of dominance among the involved allelesthe
what are universal donors and universal recipients concerning the abo blood systemthe universals donors of the abo blood type system are the
what is the logic of the transfusional compatibility concerning the abo blood group systema transfusional compatibility for the abo system takes into
what are the antigens and antibodies of each blood type of the abo blood systemtype a antigen a antibody anti-b type b antigen b antibody anti-a type
what are the blood types of the abo blood systemthe type a the type b the type ab and the type o are the blood types of the abo blood
what are the antigens and the respective antibodies of the abo blood group systemthe abo blood system contain the erythrocytic antigens a and b that
why is the determination of the blood types of the donor and of the recipient important in transfusionsthe red blood cells have different antigens in
what are the main human blood group systemsin humans the major blood group systems are the abo system the rh system and the mn
what is sex-influenced dominancethe sex-influenced dominance is the phenomenon in which the manifestation of a phenotype of a gene in heterozygosity
what are holandric genesthe holandric genes are genes situated in the nonhomologous region of the y chromosome holandric genes condition phenotypes
are sex-linked diseases associated only to genes of the x chromosomethere are so many x-linked diseases such like hemophilia b hemophilia a and
what is the type of genetic inheritance of daltonism is daltonism more frequent in men or in women what is the physiological explanation for the
what is the clinical manifestation of the disease known as daltonisman x-linked daltonism is a disease in which the affected individual sees the red
is it possible for any son of a couple formed by a hemophilic man xhy and a nonhemophilic noncarrier xx woman to be hemophilicif the mothers are not
why is it rare to find hemophilic womenthere are less hemophilic women than hemophilic men because women need to have two x chromosomes affected to
what are all possibilities of genotypes and phenotypes formed in the combination of alleles responsible for the production of factor viiiconsidering
what is the clinical deficiency presented by hemophilic people what is the genetic cause of that deficiencythe hemophilia is a disease characterized
how many alleles of genes that condition x-linked traits do female and male individuals respectively presentfor every correspondent gene to an x-
what are x-linked traitsthe x-linked traits are the phenotypical traits conditioned by genes located in the nonhomologous heterologous portions of
besides the xy system are there other sex determination systemsa few animals have a sex determination system different from the xy system such as the
what is the inactivation of the x chromosome what is a barr bodythe inactivation of the x chromosome is a phenomenon that occurs in women ever since