Splenopancreatic Field Abnormality Is Not Unique to Trisomy 13

Pediatric and Developmental Pathology

Volumn 7, Issue 1, 2004, Pages 91-94

  Peres, Luiz Cesar ^a   De Sales Barbosa, Gustavo Henrique T ^a   Careta, Renata Scarpat ^a   Nassif, Cristiane Miziara ^a   De Pina Neto, João Monteiro ^a   Giuliani, Liane R ^a   Martinhago, Ciro Dresch ^a   Gomy, Israel ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Congenital heart defect; Oligohydramnios sequence; Osteocraniostenosis syndrome; Splenopancreatic field dysplasia; Splenopancreatic fusion; Trisomy 21

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; HUMAN; INFANT; MALE; MICROPHOTOGRAPHY; MICROSCOPY; NEWBORN; PANCREAS DISEASE; PRESCHOOL CHILD; PRIORITY JOURNAL; SPLEEN; SPLEEN DISEASE; SPLENOPANCREATIC FIELD ABNORMALITY; TRISOMY 13; TRISOMY 21;

EID: 1942534646     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024-003-6067-x     Document Type: Article

References (12)

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