Human Genetics. Proceedings of the 6th International Congress..., Sept. 13-18, 1981, Jerusalem: Medical aspects. II, Teil 2Batsheva Bonné-Tamir Liss, 1982 - 619 Seiten |
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Seite 162
... occurring after age 30 ) are known as heterozygotes . Heterozygotes occur at a population frequency of about 1 in 500 persons , and homozygotes occur at a frequency of about 1 in 10 persons among European and North American populations ...
... occurring after age 30 ) are known as heterozygotes . Heterozygotes occur at a population frequency of about 1 in 500 persons , and homozygotes occur at a frequency of about 1 in 10 persons among European and North American populations ...
Seite 256
... occur within mature CML populations in that new clones arise characterized by new chromosomal changes in addition to the original CML aberration . It is thus surprising that Thomas et al ( 1979 ) cite the evidence of selection occurring ...
... occur within mature CML populations in that new clones arise characterized by new chromosomal changes in addition to the original CML aberration . It is thus surprising that Thomas et al ( 1979 ) cite the evidence of selection occurring ...
Seite 269
... occur in Bloom syndrome . Increased chromosome breakage occurs in Fanconi anemia and clones with abnormal chromosome complements have been observed in lymphocytes , skin fibroblasts , and bone marrow . However , it has not been possible ...
... occur in Bloom syndrome . Increased chromosome breakage occurs in Fanconi anemia and clones with abnormal chromosome complements have been observed in lymphocytes , skin fibroblasts , and bone marrow . However , it has not been possible ...
Inhalt
Carrier Detection | 15 |
HLA and Infectious Diseases | 37 |
HLA and Diabetes | 55 |
Urheberrecht | |
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abnormalities activity addition affected allele analysis antigens appears association binding biochemical blood carrier cells changes chromosome clinical common complex cultured defect deficiency Department determined diabetes diabetes mellitus diagnosis disease disorders distribution dominant environmental enzyme estimated et al evidence expression factors fibroblasts findings frequency gene glucose haplotypes heterogeneity heterozygotes Hum Genet human hypertension IDDM immune important increased indicated individuals inheritance internalization involved Italy levels linkage linked locus lysosomal major marker measured Medical method mode of inheritance multiple mutant neural tube normal observed occur origin pairs parents patients phenotype population possible pregnancy prenatal present problems protein recently receptor recessive relative reported Research response risk screening showed shown significant specific structure studies suggested syndrome Table tissue trait translocation tumor twin ulcer University values York