Benign familial neonatal convulsions linked to genetic markers on chromosome 20

Nature

Volumn 337, Issue 6208, 1989, Pages 647-648

  Leppert, Mark ^a   Anderson, V Elving ^b   Quattlebaum, T ^c   Stauffer, Dora ^a   O'Connell, Peter ^a   Nakamura, Yusuke ^a   Lalouel, Jean Marc ^a   White, Ray ^a  

^a UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 20; CLINICAL ARTICLE; EPILEPSY; GENETIC ENGINEERING; GENETIC LINKAGE; HEREDITY; HUMAN; LETTER; MOLECULAR GENETICS; NEWBORN; NEWBORN CONVULSION; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; CONVULSIONS; FEMALE; GENETIC MARKERS; HUMAN; INFANT, NEWBORN; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0024502803     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/337647a0     Document Type: Article

References (26)

1. Annegers, J. F., Hauser, W. A. & Anderson, V. E. In Genetic Basis of the Epilepsies (eds Anderson, V. E., Hauser, W. A., Penry, J. K. & Sing, C. F.) 151-159 (Raven, New York, 1982).
2. Bjerre, I. & Corelius, E. Acta paediat. scand. 57, 557-561 (1968).
3. McKusick, V. A. Mendelian Inheritance in Man 8th edn. 172-173 (Johns Hopkins University Press, Baltimore, 1988).
4. Rett, A. & Teubel, R. Wiener Klinische Wochenschrift 76, 609-613 (1964).
5. Zonana, J., Silvey, K. & Strimling, B. Am. J. med. Genet. 18, 455-459 (1984).
6. Gross, S., Schuber, W. & Silka, M. J. Pediat. 96, 952 (1980).
7. Dobrescu, O. & Larbrisseau, A. Can. J. neurol. Sci. 9, 345-347 (1982).
8. Takebe, Y., Chiva, C. & Kimura, S. Brain Dev. 5, 319-322 (1983).
9. Plouin, P. In Epileptic Syndromes in Infancy, Childhood and Adolescence (ed. Roger, J., Dravet, C., Bureau, M., Dreifuss, F. E. & Wolf, P.) 2-11 (John Libbey Eurotext, London, 1985).
10. Crispen, C. & Kelly, T. Iowa Med. 75, 397-401 (1985).
11. Cronin, C. & Cosgrove, J. Irish Med. J. 79, 325-326 (1986).
12. Shavell, M. I., Sinclair, D. B. & Metrakos, K. Pediat. Neurol. 2, 272-275 (1986).
13. Cunniff, C. Am. J. med. Genet. 30, 963-966 (1988).
14. Quattlebaum, T. J. Pediat. 95, 257-259 (1979).
15. Lathrop, M., Lalouel, J.-M., Julier, C. & Ott, J. Am. J. hum. Genet. 37, 482-498 (1985).
16. Giacoia, G. P. Southern Med. J. 75, 629-630.
17. Pettit, R. E. & Fenichel, G. M. In Archs Neurol. 37, 47-48.
18. Nakamura, Y. et al. Nucleic Acids Res. 16, 5222 (1988).
19. Myers, R. et al. Nucleic Acids Res. 16, 9883 (1988).
20. White, R. et al. Nature 313, 101-105 (1985).
21. Kidd, K. K. & Ott, J. Cytogenet. Cell Genet. 37, 510 (1984).
22. Conneally, P. et al. Cytogenet. Cell Genet. 40, 356-359 (1985).
23. Barker, D., Schafer, M. & White, R. Cell 36, 131-138 (1984).
24. de Martinville, B., Schafer, M., White, R. & Francke, U. Cytogenet. Cell Genet. 37, 531 (1984).
25. Goodfellow, P. J. et al. Cytogenet. Cell Genet. 44, 112-117 (1987).
26. Sparkes, R. S., Kaufman, D., Heinzmann, C., Tobin, A. J. & Mohandas, T. Cytogenet. Cell Genet. 46, 696 (1987).