oa Chromosomal Analysis in a Sample of Iraqi Children with Down's Syndrome and Concominant Cogenital Heart Disease

References

1. Hsu LYF. Parental diagnosis of chromosomal abnormalities through amniocentesis. In: Milunsky A, ed. Genetic disorder and the fetus. 4th ed..
   [Google Scholar]
2. Marino B. Congenital heart disease in patients with Down's syndrome: anatomical and genetic aspects. Biomed Pharmacother. 1993; 47:5:197–120.
   [Google Scholar]
3. Hoe TS, Chan KC, Boo NY. Cardiovascular malformation in Malaysian neonates with Down's syndrome. Singapore Med J. 1990 Oct; 31:5:474–476.
   [Google Scholar]
4. Park SC, Mathews RA, Zuberbuhler JR, Rowe RD, Neches WH, Lenox CC. Down's syndrome with congenital heart malformation. AmJDis Child. 1977 Jan; 131:1:29–33.
   [Google Scholar]
5. Laursen HB. Congenital heart disease in Down\s syndrome. Br Heart J. 1976 Jan; 38:1:32–38.
   [Google Scholar]
6. Jones KL, Smith S. Recognizable patterns of human malformation. 5th Ed. Philadelphia: WB Saunders company 1997.
   [Google Scholar]
7. Wells GL, Barker SE, Finley SC, Colvin EV, Finley WH. Congenital heart disease in infants with Down \s syndrome. South Med J. 1994 Jul; 87:7:724–727.
   [Google Scholar]
8. Granzotti JA, Panero IL, Amaral FT, Nunes MA. Incidence of heart defects in Down's syndrome. J Pediatr (Rio J). 1995 Jan-Feb; 71:1:28–30.
   [Google Scholar]
9. Nazer J, Eaglin MA, Cifuentes L. Incidence of down's syndrome at a university hospital maternity of Chile, A 25 year record:1972-1992. Rev Med CM. 1998 Apr; 126:4:383–390.
   [Google Scholar]
10. Pierpont ME, Markwald RR, Lin AF. Genetic aspects of atrioventricular septal defects. Am J Med Genet 200 Winter's;. 97:4:289–296.
    [Google Scholar]
11. Robinson SW, Morris CD, Goldmuntz E, Reller MD, Jones MA, Steiner RD, Maslen CL. Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects. Am J Hum Genet. 2003 Apr; 72:4:1047–1052.
    [Google Scholar]
12. Sandri C, Di Lisi R, Picard A, Argentini C, Calabria E, Myklak K, Scartezzini P, S . Heart morphogenesis is not affected by overexpression of the Sh3bgr gene mapping to the Down syndrome heart critical region. Hum Genet. 2004 Apr; 114:5:517–519, Epub 2004 07.
    [Google Scholar]
13. Wilson L, Curtis A, Korenberg JR, Schipper RD, Allan L, Chenevix-Trench G, Stephenson A, Goodship J, Burn J. A large, dominant pedigree of atrioventricular septal defect (AVSD): Exclusion from the Down syndrome critical region on chromosome 21. Am J Hum Genet. 1993 Dec; 53:6:1262–1268.
    [Google Scholar]
14. Thieren M, Stijns-Cailteux M, Tremouroux-Wattiez M, Jaumin P, Kestens-Servaye Y, Moulin D, Lintermans J, Vliers A. Congenital heart diseases and obstructive pulmonary vascular diseases in Down's syndrome. Apropos of 142 children with trisomy 21. Arch Mai Coeur Vaiss. 1988 May; 81:5:655–661.
    [Google Scholar]
15. Pinto FF, Nunes L, Ferraz F, Sampayo F. Down's syndrome: Different distribution of congenital heart diseases between the sexes. Int J Cardiol. 1990 May; 27:2:175–178.
    [Google Scholar]
16. Lo NS, Leung PM, Leu KC, Yeuny CY. Congenital cardiovascular malformation in Chinese children with Down's syndrome. Chin Med J (Engl). 1989 May; 102:5:382–386.
    [Google Scholar]
17. Normand J, Sassolas F, Bozio A, Jocteur-Monrozier D, Andre M. Cardiopathies in Trisomy 21. Therapeutic indications. Arch Mai Cocur Vaiss. 1981 Dec; 74:12:1427–1436.
    [Google Scholar]