Genomic imprinting and its clinical implications

New England Journal of Medicine

Volumn 326, Issue 12, 1992, Pages 827-829

  Hall, Judith G ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMNION FLUID CYTOLOGY; CHROMOSOME 15; EDITORIAL; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; MEIOSIS; PRADER WILLI SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0026560679     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJM199203193261210     Document Type: Editorial

References (8)

1. Hall J.G. Genomic imprinting. Curr Opin Genet Dev 1991; 1:34-39
2. Monk M., Surani A., eds. Genomic imprinting. Development 1990;Suppl
3. Smeets D.F.C.M., Hamel B.C.J., Nelen M.R., et al. Prader—Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15. N Engl J Med 1992; 326:807-11
4. Engel E., DeLozier-Blanchet C.D. Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection. Am J Med Genet 1991; 40:432-9
5. Cassidy S.B., Lai L.-W., Erickson R.P., et al. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. Am J Hum Genet (in press)
6. Voss R., Ben-Simon E., Avital A., et al. Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans? Am J Hum Genet 1989; 45:373-80
7. Hulten M.A., Hall J.G. On mechanisms of genomic imprinting. Chromosomes Today 1990; 10:157-62
8. Haig D., Graham C. Genomic imprinting and the strange case of the insulinlike growth factor II receptor. Cell 1991; 64:1045-6