Brain defects in infants with potter syndrome (oligohydramnios sequence)

Fetal and Pediatric Pathology

Volumn 13, Issue 4, 1993, Pages 519-536

  Kadhim, Hazim J ^a   Lammens, Martin ^b   Gosseye, Serge ^a   Gadisseux, Jean François ^a   Evrard, Philippe ^a  

^a UNIVERSITY OF LOUVAIN MEDICAL SCHOOL   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Brain anomalies; Neuronal migration; Oligohydramnios sequence; Perinatal neuropathology; Potter sequence; Potter syndrome

Indexed keywords

ARTICLE; AUTOPSY; BRAIN MALFORMATION; CLINICAL ARTICLE; DISEASE ASSOCIATION; FEMALE; HISTOPATHOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; INFANT; KIDNEY DISEASE; MALE; NERVE CELL; OLIGOHYDRAMNIOS; PATHOGENESIS; POTTER SYNDROME;

BRAIN; CELL MOVEMENT; FEMALE; HUMAN; INFANT, NEWBORN; INFANT, PREMATURE; KIDNEY; MALE; MICROSCOPY, ELECTRON; NEURONS; OLIGOHYDRAMNIOS; SUPPORT, NON-U.S. GOV'T;

EID: 0027234545     PISSN: 15513815     EISSN: None     Source Type: Journal    
DOI: 10.3109/15513819309048240     Document Type: Article

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