Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Handelin, B. L."'
Autor:
Brzustowicz, L. M., Allitto, B. A., Matseoane, D., Theve, R., Michaud, L., Chatkupt, S., Sugarman, E., Penchaszadeh, G. K., Suslak, L., Koenigsberger, M. R., Gilliam, T. C., Handelin, B. L.
Paternal isodisomy for chromosome 5 was detected in a 2-year-old boy with type III spinal muscular atrophy (SMA), an autosomal recessive degenerative disorder of alpha motor neurons, known to map to 5q11.2-13.3. Examination of 17 short-sequence repea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb80dfb2b78aed81f76ad8722ed7da40
https://europepmc.org/articles/PMC1918127/
https://europepmc.org/articles/PMC1918127/
Publikováno v:
Human molecular genetics [Hum Mol Genet] 1993 Feb; Vol. 2 (2), pp. 153-8.
Autor:
Handelin BL, Kabat D
Publikováno v:
Virology [Virology] 1985 Jan 15; Vol. 140 (1), pp. 183-7.
Publikováno v:
Science (New York, N.Y.) [Science] 1987 Jul 17; Vol. 237 (4812), pp. 268-75.