Familial heterotaxy syndrome. Case report and review of the international literature;Heterotaxia szindrómák familiáris jelentkezése. Esetismertetés és a nemzetközi irodalom áttekintése.

Orvosi hetilap

Volumn 139, Issue 46, 1998, Pages 2775-2778

  Cesko, I ^a   Hajdu J ^a   Marton, T ^a   Tarnai, L ^a   Zs Toth E ^a  

^a SEMMELWEIS UNIVERSITY OF MEDICINE   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; ECHOGRAPHY; FEMALE; FETUS DISEASE; GENETICS; HUMAN; MALE; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PREGNANCY; REVIEW; SITUS INVERSUS; SPLEEN; SYNDROME; VISCERA;

ABNORMALITIES, MULTIPLE; FEMALE; FETAL DISEASES; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; MALE; PREGNANCY; SITUS INVERSUS; SPLEEN; SYNDROME; ULTRASONOGRAPHY, PRENATAL; VISCERA;

EID: 18144442774     PISSN: 00306002     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (45)