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Volumn 37, Issue 8, 2000, Pages
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Fetal bowel hyperechogenicity may indicate mild atypical cystic fibrosis: a case associated with a complex CFTR allele.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
CFTR PROTEIN, HUMAN;
TRANSMEMBRANE CONDUCTANCE REGULATOR;
ADULT;
ALLELE;
CASE REPORT;
CHILD;
CYSTIC FIBROSIS;
FEMALE;
GENETIC COUNSELING;
GENETICS;
HETEROZYGOTE;
HUMAN;
INTESTINE;
LETTER;
MALE;
MUTATION;
NEWBORN;
PREGNANCY;
PRENATAL DEVELOPMENT;
PRESCHOOL CHILD;
ADULT;
ALLELES;
CHILD;
CHILD, PRESCHOOL;
CYSTIC FIBROSIS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
FEMALE;
GENETIC COUNSELING;
HETEROZYGOTE;
HUMANS;
INFANT, NEWBORN;
INTESTINES;
MALE;
MUTATION;
PREGNANCY;
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EID: 17144467755
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.37.8.e15 Document Type: Letter |
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Times cited : (8)
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References (0)
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