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 240
... Chromosomal localization of human immunoglobulin light chain constant region genes . Human Gene Mapping Conference ... abnormalities in cancer . Cancer Genet Cytogenet 2 : 175–198 . Rowley JD , Golomb HM , Vardiman J , Fukuhara S , Dougherty ...
... Chromosomal localization of human immunoglobulin light chain constant region genes . Human Gene Mapping Conference ... abnormalities in cancer . Cancer Genet Cytogenet 2 : 175–198 . Rowley JD , Golomb HM , Vardiman J , Fukuhara S , Dougherty ...
Seite 356
... chromosomal aberrations such as chromatid breaks are the direct result ... abnormalities like those seen in A - T ( Hustinx et al , 1979 ) . However ... chromosomal abnormalities in sequential cytogenetic studies of ataxia telangiectasia ...
... chromosomal aberrations such as chromatid breaks are the direct result ... abnormalities like those seen in A - T ( Hustinx et al , 1979 ) . However ... chromosomal abnormalities in sequential cytogenetic studies of ataxia telangiectasia ...
Seite 531
... chromosomal aberration in the parents . In Murken JD , Stengel - Rutkowski S , Schwinger E ( eds ) : “ Prenatal Diagnosis . " Stuttgart : Enke , pp 1-14 . Boué J , Morer I , Vignal P ( 1980 ) : Tentative definition of a chromosomal anomaly ...
... chromosomal aberration in the parents . In Murken JD , Stengel - Rutkowski S , Schwinger E ( eds ) : “ Prenatal Diagnosis . " Stuttgart : Enke , pp 1-14 . Boué J , Morer I , Vignal P ( 1980 ) : Tentative definition of a chromosomal anomaly ...
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