Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome

Prenatal Diagnosis

Volumn 22, Issue 8, 2002, Pages 692-696

  Rousseau, Thierry ^a   Laurent, Nicole ^a   Thauvin Robinet, Christel ^a   Lionnais, Stéphanie ^a   Durand, Christine ^a   Faivre, Laurence ^a   Sagot, Paul ^a  

^a DIJON UNIVERSITY HOSPITAL   (France)

Author keywords

Autosomal recessive inheritance; Cryptophthalmos syndrome; Fraser syndrome; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CLINICAL FEATURE; EYE MALFORMATION; FAMILIAL DISEASE; FEMALE; FRASER SYNDROME; GENETIC DISORDER; GENETIC HETEROGENEITY; HUMAN; KIDNEY AGENESIS; MULTIGENE FAMILY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SYNDACTYLY; CONGENITAL MALFORMATION; DENYS DRASH SYNDROME; ECHOGRAPHY; EYELID; FATALITY; FEMALE GENITAL SYSTEM; GENETICS; GESTATIONAL AGE; KIDNEY; MALE; MULTIPLE MALFORMATION SYNDROME; OLIGOHYDRAMNIOS; PREGNANCY; URETER;

ABNORMALITIES, MULTIPLE; CASE REPORT; DENYS-DRASH SYNDROME; EYELIDS; FATAL OUTCOME; FEMALE; GENITALIA, FEMALE; GESTATIONAL AGE; HUMAN; KIDNEY; MALE; OLIGOHYDRAMNIOS; PREGNANCY; SYNDACTYLY; ULTRASONOGRAPHY, PRENATAL; URETER; HUMANS;

EID: 0036023283     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.381     Document Type: Article

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22. Eine Missgeburt mit hautüberwachsenen augen oder kryptophthalmus