Family, Population and Mother-Child Studies of Two Phosphoglucomutase Loci (PCM1and PGM3)
作者:
L.U. Lamm,
期刊:
Human Heredity
(Karger Available online 1970)
卷期:
Volume 20,
issue 3
页码: 292-304
ISSN:0001-5652
年代: 1970
DOI:10.1159/000152325
出版商: S. Karger AG
关键词: Phosphoglucomutase loci PGMXand PGM3;Population and family studies;Linkage analysis
数据来源: Karger
摘要:
Studies on PGMj and PGM3 isozymes in leucocytes from 110 matings with 383 children and 138 mother-child combinations support the hypothesis that these characters are determined by codominant alleles at two separate loci. The two characters were found to be fully developed in leucocytes at birth. The frequency in Denmark of the least common allele at the two loci is 0.19 for PGMJ and 0.25 for PGM∣. The two loci PGM]^ and PGM3 showed no indication of linkage or association and may therefore be regarded as independent markers. A pedigree of a family with the rare PGM* allele is presente
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