Exclusion of chromosomal abnormalities and microdeletions 22q11 and 10p13 in algerian patients with isolated conotruncal malformation

Author:

Ammar-Khodja F.,Abdellali M.

Publisher

Allerton Press

Subject

Genetics,Agricultural and Biological Sciences (miscellaneous),Cell Biology

Reference50 articles.

1. Hofmann, J.I.E. and Kaplan, S., The incidence of congenital heart disease and its prevalence in adults, Br. Heart J., 1962, vol. 24, pp. 557–560.

2. Johnson, M.C., Hing, A., Wood, M.K., and Watsor, M.S., Chromosomes abnormalities in congenital heart disease, Am. J. Med. Genet., 1997, vol. 70, pp. 292–298.

3. Di-George, A.M., Congenital absence of the thymus and its immunologic consequence: concurrence with congenital hypoparathyroidism, in Immunologic Deficiency Disease in Man, in Birth Defects: Original Article Series, Bergsman, D. and Good, R.A., Eds., New York: Natl. Found. Press, 1968, vol. 4, no. 1, pp. 116–121.

4. Shprintzen, R.J., Goldberg, R.B., Lewin, M.L., et al., New syndrome involving cleft palate, cardiac anomalies typical facies and learning disabilities: velo-cardiofacial syndrome, Cleft Palate J., 1978, vol. 15, p. 56.

5. Burn, J., Takao, A., Wilson, D., et al., Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11, Am. J. Med. Genet., 1993, vol. 30, pp. 822–824.

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