BIOMAT Database Logo BIOMAT Database Logo

A rare phosphoglucomutase phenotype: pgm1 6--1. 1975

J Gerchow, and D Mebs

UI MeSH Term Description Entries
D008297 Male Males
D010334 Paternity Establishing the father relationship of a man and a child. Paternities
D010641 Phenotype The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment. Phenotypes
D010733 Phosphoglucomutase An enzyme that catalyzes the conversion of alpha D-glucose 1-phosphate to alpha D-glucose 6-phosphate. EC 5.4.2.2. Glucose Phosphomutase,Phosphomutase, Glucose
D011110 Polymorphism, Genetic The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level. Gene Polymorphism,Genetic Polymorphism,Polymorphism (Genetics),Genetic Polymorphisms,Gene Polymorphisms,Polymorphism, Gene,Polymorphisms (Genetics),Polymorphisms, Gene,Polymorphisms, Genetic
D004912 Erythrocytes Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. Blood Cells, Red,Blood Corpuscles, Red,Red Blood Cells,Red Blood Corpuscles,Blood Cell, Red,Blood Corpuscle, Red,Erythrocyte,Red Blood Cell,Red Blood Corpuscle
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

J Gerchow, and D Mebs
Rare phosphoglucomutase phenotypes PGM1 3-1 and PGM1 3-2 in the Polish population. A case report.
January 1979, Forensic science international,
J Gerchow, and D Mebs
The rare PGM1 7-1 phenotype in a Polish family.
January 1977, Archivum immunologiae et therapiae experimentalis,
J Gerchow, and D Mebs
Rare alleles of phosphoglucomutase (PGM1) in the Polish population.
January 1989, Archivum immunologiae et therapiae experimentalis,
J Gerchow, and D Mebs
Isoelectric focusing of human red cell phosphoglucomutase (PGM1): phenotype distribution in the Swiss population - rare phenotypes.
January 1981, Human heredity,
J Gerchow, and D Mebs
Identification of a rare allele of phosphoglucomutase (PGM1) in an Italian family.
October 1975, Humangenetik,
J Gerchow, and D Mebs
[Genetic studies of phosphoglucomutase-1 (PGM1) subtypes: population aspects].
April 1991, Genetika,
J Gerchow, and D Mebs
[Rare PGM1 (6) and PGM1(7) alleles in the Polish population].
January 1984, Zeitschrift fur Rechtsmedizin. Journal of legal medicine,
J Gerchow, and D Mebs
A new partially deficient variant in the phosphoglucomutase 1 system, PGM1*W31.
February 1986, Human genetics,
J Gerchow, and D Mebs
Phosphoglucomutase-1 subtypes in two populations in Adriatic islands: presence of PGM1*W3 (PGM1*7+) allele.
January 1991, Human heredity,
J Gerchow, and D Mebs
Identification of base substitutions in ten types of rare variants of phosphoglucomutase-1 (PGM1) encountered in Japanese.
October 2001, Human biology,
Copied contents to your clipboard!