Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation.

Journal of medical genetics

Volumn 41, Issue 5, 2004, Pages

  Ogino, S ^a   Wilson, R B ^a   Grody, W W ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; BAYES THEOREM; CYSTIC FIBROSIS; ECHOGRAPHY; FEMALE; GENETIC DISORDER; GENETIC SCREENING; GENETICS; HETEROZYGOTE; HUMAN; INTESTINE; MUTATION; NUCLEOTIDE SEQUENCE; PARENT; PREGNANCY; RECESSIVE GENE; RISK ASSESSMENT;

BAYES THEOREM; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, RECESSIVE; GENETIC DISEASES, INBORN; GENETIC SCREENING; HETEROZYGOTE; HUMANS; INTESTINES; MUTATION; PARENTS; PREGNANCY; RISK ASSESSMENT; ULTRASONOGRAPHY, PRENATAL;

EID: 3042769509     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2003.015065     Document Type: Article

References (0)