Tracking Rare Incidence Syndromes (TRIS) project [3]

American Journal of Medical Genetics, Part A

Volumn 140, Issue 22, 2006, Pages 2510-

  Bruns, Deborah A ^a  

^a SOUTHERN ILLINOIS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME DISORDER; CONGENITAL MALFORMATION; DATA BASE; DECISION MAKING; FAMILY; HEALTH EDUCATION; HEALTH PROGRAM; HUMAN; INCIDENCE; LETTER; MEDICAL GENETICS; PRIORITY JOURNAL; SYNDROME; TRACKING RARE INCIDENCE SYNDROME PROJECT; TRISOMY 18;

CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; HUMANS; PILOT PROJECTS; SYNDROME; TRISOMY;

EID: 33750582207     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31512     Document Type: Letter

References (4)

1. Kosho T, Nakamura T, Kawame H, Baba A. Tamura M, Fukushima Y. 2006. Neonatal management of trisomy 18: Clinical details of 24 patients receiving intensive treatment. Am J Med Genet Part A 140A:937-944.
2. Lin H-Y, Lin S-P, Chen Y-J, Hung H-Y, Kao H-A, Hsu C-H, Chen M-R, Chang J-H, Ho C-S, Huang F-Y, Shyur S-D, Lin D-S, Lee H-C. 2006, Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004. Am J Med Genet Part A 140A:945-951.
3. Niedrist D, Riegel M, Achermann J, Schinzel A. 2006. Survival with trisomy 18-Data from Switzerland. Am J Med Genet Part A 140A:952-959.
4. Pont SJ, Robbins JM, Bird TM, Gibson JB, Cleves MA, Tilford JM, Aitken ME. 2006. Congenital malformations among liveborn infants with trisomies 18 and 13. Am J Med Genet Part A 140A:1749-1756.