Aberrant Nuclear Projections of Neutrophils in Trisomy 13

Archives of Pathology and Laboratory Medicine

Volumn 128, Issue 2, 2004, Pages 243-244

  Salama, Mohamed E ^a   Shah, Veena ^a   Lebel, Robert Roger ^a   VanDyke, Daniel L ^a  

^a HENRY FORD HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CELL NUCLEUS; CLINICAL FEATURE; FALLOT TETRALOGY; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; HUMAN; HYPOTENSION; HYPOXEMIA; MATERNAL BLOOD; NEUTROPHIL; NEWBORN; NEWBORN DEATH; POLYDACTYLY; PRENATAL DIAGNOSIS; RESPIRATORY DISTRESS; TRISOMY 13;

ADULT; CELL NUCLEUS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 13; FEMALE; HUMANS; NEUTROPHILS; TRISOMY;

EID: 0742287339     PISSN: 00039985     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Baty BJ, Brent BL, Carey JC. Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence risk. Am J Med Genet. 1994;49:175-188.
2. 1 (13-15) trisomy syndrome. Lancet 1964;13:589-590.
3. Walzer S, Gerald PS, Breau G, O'Neill D, Diamond LK. Hematologic changes in the trisomy syndrome. Pediatrics. 1966;38:419-429.