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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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