Norman-Roberts syndrome: Prenatal diagnosis and autopsy findings

Prenatal Diagnosis

Volumn 20, Issue 6, 2000, Pages 505-509

  Sergi, Consolato ^a   Zoubaa, Saida ^b   Schiesser, Monika ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b NONE

Author keywords

Lissencephaly type I; Norman Roberts syndrome

Indexed keywords

AGYRIA; ARTICLE; AUTOPSY; BIPARIETAL DISTANCE; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 17P; CONSANGUINEOUS MARRIAGE; ECHOGRAPHY; EYE MALFORMATION; FEMALE; FEMUR; FETUS; HEAD CIRCUMFERENCE; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; INTRAUTERINE GROWTH RETARDATION; KARYOTYPE; MALE; MICROCEPHALY; MILLER DIEKER SYNDROME; NOSE MALFORMATION; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING; SKULL MALFORMATION; SYNDROME DELINEATION;

ACRONICTA LEPORINA; SYLVIA;

EID: 0034049913     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0223(200006)20:6<505::aid-pd850>3.0.co;2-%23     Document Type: Article

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