Vnd, a gene required for early neurogenesis of Drosophila, encodes a homeodomain protein
Jimenez, F, Martin-Morris, L.E, Velasco, L, Chu, H, Sierra, J, Rosen, D.R, White, K
Published in The EMBO journal (17.07.1995)
Published in The EMBO journal (17.07.1995)
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Journal Article
An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia
Higgins, J J, Loveless, J M, Goswami, S, Nee, L E, Cozzo, C, De Biase, A, Rosen, D R
Published in Neurology (12.06.2001)
Published in Neurology (12.06.2001)
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Journal Article
Assignment of SOD3 to human chromosome band 4p15.3→p15.1 with somatic cell and radiation hybrid mapping, linkage mapping, and fluorescent in-situ hybridization
Stern, L.F., Chapman, N.H., Wijsman, E.M., Altherr, M.R., Rosen, D.R.
Published in Cytogenetic and genome research (2003)
Published in Cytogenetic and genome research (2003)
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Journal Article
Genetic mapping of GLCLC, the human gene encoding the catalytic subunit of gamma-glutamylcysteine synthetase, to chromosome band 6p12 and characterization of a polymorphic trinucleotide repeat within its 5' untranslated region
Walsh, A C, W Li, Rosen, D R, Lawrence, D A
Published in Cytogenetic and genome research (01.01.1996)
Published in Cytogenetic and genome research (01.01.1996)
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Journal Article
Human Ciliary Neurotrophic Factor: Localization to the Proximal Region of the Long Arm of Chromosome 11 and Association with CA/GT Dinucleotide Repeat
Lev, A.A., Rosen, D.R., Kos, C., Clifford, E., Landes, G., Hauser, S.L., Brown, R.H.
Published in Genomics (San Diego, Calif.) (01.05.1993)
Published in Genomics (San Diego, Calif.) (01.05.1993)
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Journal Article
Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1)
Donaldson, D H, Rosen, D R, O'Regan, J, Sapp, P C, Horvitz, H R, Gusella, J F, Haines, J L, Pestka, S, Jung, V, Nusbaum, C
Published in Human molecular genetics (01.10.1992)
Published in Human molecular genetics (01.10.1992)
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Journal Article
Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1
Rosen, D R, Sapp, P C, O'Regan, J, Horvitz, H R, Donaldson, D H, Nussbaum, C, Gusella, J F, Haines, J L, Pestka, S, Jung, V
Published in Human molecular genetics (01.10.1992)
Published in Human molecular genetics (01.10.1992)
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Genetic anticipation in a large family with pure autosomal dominant hereditary spastic paraplegia
Thurmon, T F, He, C, Haskell, C, Thorpe, P, Thurmon, S G, Rosen, D R
Published in American journal of medical genetics (23.04.1999)
Published in American journal of medical genetics (23.04.1999)
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Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers
Rosen, D R, Sapp, P, O'Regan, J, McKenna-Yasek, D, Schlumpf, K S, Haines, J L, Gusella, J F, Horvitz, H R, Brown, Jr, R H
Published in American journal of medical genetics (15.05.1994)
Published in American journal of medical genetics (15.05.1994)
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