Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
Ergebnisse 1-3 von 34
Seite 149
... locus , the Sandhoff variant as a mutation at the ẞ - polypeptide locus , and the puzzling AB variant with gangliosidosis and CNS disease , yet with normal hexosaminidase activity when assayed with artificial substrate , as a possible ...
... locus , the Sandhoff variant as a mutation at the ẞ - polypeptide locus , and the puzzling AB variant with gangliosidosis and CNS disease , yet with normal hexosaminidase activity when assayed with artificial substrate , as a possible ...
Seite 297
... locus B locus C locus D locus HLA - A1 A2 22 92 16 HLA - B5 4 HLA - CW1 BW35 8 CW2 A28 6 B18 5 CW3 A3 14 B7 12 CW4 All 9 BW22 3 CW5 A9 JAW23 2 B8 13 Blank 74 mmaont 3 HLA - DW1 3 10 DW2 8 9 DW3 9 6 DW4 8 5 DW5 7 DW6 5 AW24 7 B12 12 ...
... locus B locus C locus D locus HLA - A1 A2 22 92 16 HLA - B5 4 HLA - CW1 BW35 8 CW2 A28 6 B18 5 CW3 A3 14 B7 12 CW4 All 9 BW22 3 CW5 A9 JAW23 2 B8 13 Blank 74 mmaont 3 HLA - DW1 3 10 DW2 8 9 DW3 9 6 DW4 8 5 DW5 7 DW6 5 AW24 7 B12 12 ...
Seite 319
... locus ( Ss ) and one Class IV locus ( H - 2G ) . Preliminary and limited amino acid sequence data available for the products of some of these loci indicate that the two Class I loci are homologous and most likely arose by gene ...
... locus ( Ss ) and one Class IV locus ( H - 2G ) . Preliminary and limited amino acid sequence data available for the products of some of these loci indicate that the two Class I loci are homologous and most likely arose by gene ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel