C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response

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Standard

C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response. / Schiøtz, P O; Høiby, N; Morling, N; Sørensen, H.

In: Human Heredity, Vol. 28, No. 4, 1978, p. 293-300.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Schiøtz, PO, Høiby, N, Morling, N & Sørensen, H 1978, 'C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response', Human Heredity, vol. 28, no. 4, pp. 293-300.

APA

Schiøtz, P. O., Høiby, N., Morling, N., & Sørensen, H. (1978). C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response. Human Heredity, 28(4), 293-300.

Vancouver

Schiøtz PO, Høiby N, Morling N, Sørensen H. C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response. Human Heredity. 1978;28(4):293-300.

Author

Schiøtz, P O ; Høiby, N ; Morling, N ; Sørensen, H. / C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response. In: Human Heredity. 1978 ; Vol. 28, No. 4. pp. 293-300.

Bibtex

@article{91c82ef0328c11df8ed1000ea68e967b,

title = "C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response",

abstract = "The C3 types of human serum are reported for a material of 113 Danish cystic fibrosis patients, age 0-30 years. The frequency of the C3F gene was 0.2832 which was significantly higher (p less than 0.0005) than the frequency found in a control group of 224 healthy babies (C3F = 0.1585). It also differed significantly (p less than 0.01) from the C3F gene frequency of 0.1780 found in 177 blood donors, age 20-24 years. A significant association between any of the C3 phenotypes and the most serious infection in cystic fibrosis, chronic mucoid P. aeruginosa infection, or the antibody response against these bacteria was not found.",

author = "Schi{\o}tz, {P O} and N H{\o}iby and N Morling and H S{\o}rensen",

note = "Keywords: Adolescent; Adult; Antibodies, Bacterial; Child; Child, Preschool; Complement C3; Cystic Fibrosis; Denmark; Female; Gene Frequency; Humans; Infant; Infant, Newborn; Male; Phenotype; Polymorphism, Genetic; Pseudomonas Infections",

year = "1978",

language = "English",

volume = "28",

pages = "293--300",

journal = "Human Heredity",

issn = "0001-5652",

publisher = "S Karger AG",

number = "4",

}

RIS

TY - JOUR

T1 - C3 polymorphism in a Danish cystic fibrosis population and its possible association with antibody response

AU - Schiøtz, P O

AU - Høiby, N

AU - Morling, N

AU - Sørensen, H

N1 - Keywords: Adolescent; Adult; Antibodies, Bacterial; Child; Child, Preschool; Complement C3; Cystic Fibrosis; Denmark; Female; Gene Frequency; Humans; Infant; Infant, Newborn; Male; Phenotype; Polymorphism, Genetic; Pseudomonas Infections

PY - 1978

Y1 - 1978

N2 - The C3 types of human serum are reported for a material of 113 Danish cystic fibrosis patients, age 0-30 years. The frequency of the C3F gene was 0.2832 which was significantly higher (p less than 0.0005) than the frequency found in a control group of 224 healthy babies (C3F = 0.1585). It also differed significantly (p less than 0.01) from the C3F gene frequency of 0.1780 found in 177 blood donors, age 20-24 years. A significant association between any of the C3 phenotypes and the most serious infection in cystic fibrosis, chronic mucoid P. aeruginosa infection, or the antibody response against these bacteria was not found.

AB - The C3 types of human serum are reported for a material of 113 Danish cystic fibrosis patients, age 0-30 years. The frequency of the C3F gene was 0.2832 which was significantly higher (p less than 0.0005) than the frequency found in a control group of 224 healthy babies (C3F = 0.1585). It also differed significantly (p less than 0.01) from the C3F gene frequency of 0.1780 found in 177 blood donors, age 20-24 years. A significant association between any of the C3 phenotypes and the most serious infection in cystic fibrosis, chronic mucoid P. aeruginosa infection, or the antibody response against these bacteria was not found.

M3 - Journal article

C2 - 658974

VL - 28

SP - 293

EP - 300

JO - Human Heredity

JF - Human Heredity

SN - 0001-5652

IS - 4

ER -

ID: 18693778