|
|
|
Volumn 38, Issue 7, 1991, Pages 461-467
|
|
A contribution to the genetic study of congenital afibrinogemeia. Review of twelve cases;CONTRIBUTION A L'ETUDE GENETIQUE DE L'AFIBRINOGENEMIE CONGENITALE. A PROPOS DE DOUZE CAS
a a a a a a a |
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
AFIBRINOGENEMIA;
ARTICLE;
AUTOSOMAL RECESSIVE INHERITANCE;
CLINICAL ARTICLE;
CONGENITAL DISORDER;
CONSANGUINITY;
FEMALE;
HUMAN;
MALE;
PRESCHOOL CHILD;
BLOOD;
CASE REPORT;
CHEMISTRY;
GENETIC COUNSELING;
GENETIC SCREENING;
GENETIC VARIABILITY;
GENETICS;
HETEROZYGOTE DETECTION;
INFANT;
NEWBORN;
PEDIGREE;
PHENOTYPE;
RECESSIVE GENE;
FIBRINOGEN;
AFIBRINOGENEMIA;
CASE REPORT;
CONSANGUINITY;
ENGLISH ABSTRACT;
FEMALE;
FIBRINOGEN;
GENES, RECESSIVE;
GENETIC COUNSELING;
GENETIC SCREENING;
HETEROZYGOTE DETECTION;
HUMAN;
INFANT;
INFANT, NEWBORN;
MALE;
PEDIGREE;
PHENOTYPE;
VARIATION (GENETICS);
|
|
EID: 0025900748
PISSN: 00662097
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
|
Times cited : (8)
|
|
References (0)
|